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Recalls affecting Illinois

Data last updated: September 7, 2026 at 12:15 AM UTC

17,179 recalls found

Just announced

Straight from FDA press releases — not yet formally classified or risk-graded
UnclassifiedUndeclaredAnnounced September 4, 2026

Business Pill, Branch Manager for Men — dietary supplements marketed for male sexual enhancement

Products contain undeclared yohimbine

▸Full report
Dietary SupplementsFood & Beverages

Recalling firm: SUPPLX.com

Grant-Valkaria, Florida - SUPPLX.com is voluntarily recalling Business Pill and Branch Manager for Men, products marketed as dietary supplements for male sexual enhancement, because FDA laboratory analysis confirmed that both products contain yohimbine that is not declared on the product labels.

Company contact: (321) 341-9501 · SupplxRecall@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced September 4, 2026

Foods Alive — Moringa Leaf Powder

Potential to be contaminated with Salmonella

▸Full report
Food & BeveragesFoodborne Illness

Recalling firm: Foods Alive Inc.

Foods Alive Inc of Angola, IN, is recalling its 8-ounce packages of organic moringa leaf powder because they have the potential to be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced September 3, 2026

B. Braun — 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container

Presence of particulate matter identified as iron oxide

▸Full report
Drugs

Recalling firm: B. Braun Medical Inc.

“On September 3, 2026 firm updated their press release to include additional contaminants.” FOR IMMEDIATE RELEASE – September 3, 2026– Bethlehem, PA, B. Braun Medical Inc (B. Braun) is voluntarily recalling three (3) lots of 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container, to the hospital/healthcare facility/user level due to presence of particulate matter identified as iron…

Company contact: recalls@bbraunusa.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced September 3, 2026

Great Value — Organic Triple Berry Blend

Possible E. Coli Contamination

▸Full report
Food & BeveragesFoodborne Illness

Recalling firm: Frutas y Hortalizas del Sur S.A.

September 02, 2026. Frutas y Hortalizas del Sur S.A., San Carlos, Chile expands its July 3, 2026, recall of frozen organic IQF blueberries to include one lot of Great Value frozen Organic Triple Berry Blend 10 OZ because of potential contamination with Escherichia coli O145:H28 (E. coli O145) .

Company contact: Info.foodsafety@comfrut.com

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced September 3, 2026

American Regent, Inc. — Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vial

Presence of particulate matter and lack of sterility assurance

▸Full report
Food & Beverages

Recalling firm: American Regent, Inc.

FOR IMMEDIATE RELEASE – September 3, 2026 – New Albany, OH, American Regent, Inc. is conducting a nationwide voluntary recall of three lots of Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vials to the consumer level. Customer complaints were received for leaking and cracked vials, resulting in lack of assurance of sterility.

View FDA’s announcement (opens in a new tab)
UnclassifiedUndeclaredAnnounced August 31, 2026

Lipofit — Lipofit Extreme 2.0 Fat Burner Dietary Supplement

Undeclared Fluoxetine and 2,4-Dinitrophenol (DNP)

▸Full report
Dietary SupplementsDrugs

Recalling firm: Ana Salazar Modela Tu Cuerpo Inc.

FOR IMMEDIATE RELEASE - August 27, 2026 - Davie, Florida – Ana Salazar Modela Tu Cuerpo Inc. is recalling Lipofit Extreme Fat Burner 2.0, Lot 25M12F, expiration date 09/2027, to the consumer level.

Company contact: (954) 305-1004 · yandrydy@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced August 31, 2026

Kofinas — Garlic Mediterranean Infused Extra Virgin Olive Oil 500 ml, 250 ml, and 100 ml

Contains garlic essential oil not approved for culinary use

▸Full report
Food & BeveragesIngredients

Recalling firm: LMSI LLC

Cincinnati, OH (Aug. 29, 2026) - LMSI LLC/ Kofinas Olive Oil is issuing a voluntary recall of its Garlic Mediterranean infused extra virgin olive oil for using a garlic essential oil not approved for culinary use. The flavored oil was bottled in glass bottles in 500 ml, 250 ml, and 100 ml sizes.

View FDA’s announcement (opens in a new tab)
UnclassifiedAllergenUndeclaredAnnounced August 31, 2026

Little Temptations — Chocolatey Eyeballs, 7 oz., 10 oz., 10.5 oz., 11 oz., and 16 oz.

Undeclared milk

▸Full report
Food & BeveragesAllergens

Recalling firm: Crystal Temptations

Crystal Temptations of North Arlington, NJ is recalling Halloween Chocolatey Eyeballs because they contain undeclared MILK allergens. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced August 29, 2026

Everything Sprouts — Robust Radish Mix, 5oz Cups

Potential to be contaminated with Shiga toxin-producing Escherichia coli (STEC) or Salmonella.

▸Full report
Food & BeveragesFoodborne Illness

Recalling firm: Everything Sprouts, LLC

Everything Sprouts, LLC, based in Minneapolis, MN is expanding its voluntary recall of sprouts to include certain lots of Robust Radish Sprout Mix because it has the potential to be contaminated with Shiga toxin producing Escherichia coli (STEC) or Salmonella bacteria.

Company contact: everythingsproutsmn@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced August 29, 2026

Martina — Mangoes

Potential contamination with Salmonella

▸Full report
Food & BeveragesFoodborne Illness

Recalling firm: Panorama Produce

MAMARONECK, NY, AUG. 28, 2026 - Panorama Produce is recalling 302 boxes of size 9 (nine) mangoes because they may be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

Company contact: information@panoramaproduce.com

View FDA’s announcement (opens in a new tab)
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Wording
Class IHigh risk
FoodBacteria/virusRecalled April 20, 2026

Low Heat Non-Fat Dried Milk Powder - paper bags 25 kg. (packed under 5 labels: Off Grade NFDM Variable; Extra Grade NFDM Standard rBST Free; Grade A NFDM LH Basic; Grade A NFDM LH Standard rBST Free; Grade A NFDM LH Tier 1 rBST Free)

Potential contamination with Salmonella.

ALL 50 STATES
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-0699-2026
Lot/product code:
Batch Codes for recalled product all start with A or B full list below. Batch Codes and Production Date: B22725-01-A 8/15/2025; B22725-01-B 8/15/2025; B22725-01-C 8/15/2025; B22725-01-D 8/15/2025; B22725-01-E 8/15/2025; B22725-01-F 8/15/2025; B22725-01-G 8/15/2025; B22725-01-H 8/15/2025; B22825-01-A 8/16/2025; B22825-01-B 8/16/2025; B22825-02-A 8/16/2025; B22825-02-B 8/16/2025; B22825-02-C 8/16/2025; B22825-02-D 8/16/2025; B22825-02-E 8/16/2025; B22825-02-F 8/16/2025; B22825-02-G 8/16/2025; B22825-02-H 8/16/2025; B22825-03-A 8/16/2025; B22825-03-B 8/16/2025; B22825-03-C 8/16/2025; B22825-03-D 8/16/2025; B22825-03-E 8/16/2025; B22825-03-F 8/16/2025; B22825-03-G 8/16/2025; B22825-03-H 8/16/2025; B22825-04-A 8/16/2025; B22825-04-B 8/16/2025; B22825-04-C 8/16/2025; B22825-04-D 8/16/2025; B22825-04-E 8/16/2025; B22825-04-F 8/16/2025; B22825-04-G 8/16/2025; B22825-04-H 8/16/2025; B22825-05-A 8/16/2025; B22825-05-B 8/16/2025; B22825-05-C 8/16/2025; B22825-05-D 8/16/2025; B22825-05-E 8/16/2025; B22825-05-F 8/16/2025; B22825-05-G 8/16/2025; B22825-05-H 8/16/2025; B22925-05-A 8/17/2025; B22925-05-B 8/17/2025; B22925-05-C 8/17/2025; B22925-05-D 8/17/2025; B22925-05-E 8/17/2025; B22925-05-F 8/17/2025; B22925-05-G 8/17/2025; B22925-05-H 8/17/2025; B22925-06-A 8/17/2025; B22925-06-B 8/17/2025; B22925-06-C 8/17/2025; B22925-06-D 8/17/2025; B22925-06-E 8/17/2025; B22925-06-F 8/17/2025; B22925-06-G 8/17/2025; B22925-06-H 8/17/2025; B23025-01-A 8/18/2025; B23025-01-B 8/18/2025; B23025-01-C 8/18/2025; B23025-01-D 8/18/2025; B23025-01-E 8/18/2025; B23025-01-F 8/18/2025; B23025-01-G 8/18/2025; B23025-01-H 8/18/2025; B23025-02-A 8/18/2025; B23025-02-B 8/18/2025; B23025-02-C 8/18/2025; B23025-02-D 8/18/2025; B23025-02-E 8/18/2025; B23025-02-F 8/18/2025; B23025-02-G 8/18/2025; B23025-02-H 8/18/2025; B23025-03-A 8/18/2025; B23025-03-B 8/18/2025; B23025-03-C 8/18/2025; B23025-03-D 8/18/2025; B23025-03-E 8/18/2025; B23025-03-F 8/18/2025; B23025-03-G 8/18/2025; B23025-03-H 8/18/2025; B23025-04-A 8/18/2025; B23025-04-B 8/18/2025; B23025-04-C 8/18/2025; B23025-04-D 8/18/2025; B23025-04-E 8/18/2025; B23025-04-F 8/18/2025; B23025-04-G 8/18/2025; B23025-04-H 8/18/2025; B23125-10-A 8/19/2025; B23125-10-B 8/19/2025; B23125-10-C 8/19/2025; B23125-10-D 8/19/2025; B23125-10-E 8/19/2025; B23125-10-F 8/19/2025; B23125-10-G 8/19/2025; B23125-10-H 8/19/2025; B23425-02-A 8/22/2025; B23425-02-B 8/22/2025; B23425-02-C 8/22/2025; B23425-02-D 8/22/2025; B23425-02-E 8/22/2025; B23425-02-F 8/22/2025; B23425-02-G 8/22/2025; B23425-02-H 8/22/2025; B23425-03-A 8/22/2025; B23425-03-B 8/22/2025; B23425-03-C 8/22/2025; B23425-03-D 8/22/2025; B23425-03-E 8/22/2025; B23425-03-F 8/22/2025; B23425-03-G 8/22/2025; B23425-03-H 8/22/2025; B23625-01-A 8/24/2025; B23625-01-B 8/24/2025; B23625-01-C 8/24/2025; B23625-01-D 8/24/2025; B23625-01-E 8/24/2025; B23625-01-F 8/24/2025; B23625-01-G 8/24/2025; B23625-01-H 8/24/2025; B23625-02-A 8/24/2025; B23625-02-B 8/24/2025; B23625-02-C 8/24/2025; B23625-02-D 8/24/2025; B23625-02-E 8/24/2025; B23625-02-F 8/24/2025; B23625-02-G 8/24/2025; B23625-02-H 8/24/2025; B23925-05-A 8/27/2025; B23925-05-B 8/27/2025; B23925-05-C 8/27/2025; B23925-05-D 8/27/2025; B23925-05-E 8/27/2025; B23925-05-F 8/27/2025; B23925-05-G 8/27/2025; B23925-05-H 8/27/2025; B23925-06-A 8/27/2025; B23925-06-B 8/27/2025; B23925-06-C 8/27/2025; B23925-06-D 8/27/2025; B23925-06-E 8/27/2025; B23925-06-F 8/27/2025; B23925-06-G 8/27/2025; B23925-06-H 8/27/2025; B24025-06-A 8/28/2025; B24025-06-B 8/28/2025; B24025-06-C 8/28/2025; B24025-06-D 8/28/2025; B24025-06-E 8/28/2025; B24025-06-F 8/28/2025; B24025-06-G 8/28/2025; B24025-06-H 8/28/2025; B24025-07-A 8/28/2025; B24025-07-B 8/28/2025; B24025-07-C 8/28/2025; B24025-07-D 8/28/2025; B24025-07-E 8/28/2025; B24025-07-F 8/28/2025; B24025-07-G 8/28/2025; B24025-07-H 8/28/2025; B24125-01-A 8/29/2025; B24125-01-B 8/29/2025; B24125-01-C 8/29/2025; B24125-01-D 8/29/2025; B24125-01-E 8/29/2025; B24125-01-F 8/29/2025; B24125-01-G 8/29/2025; B24125-01-H 8/29/2025; B24125-02-A 8/29/2025; B24125-02-B 8/29/2025; B24125-02-C 8/29/2025; B24125-02-D 8/29/2025; B24125-02-E 8/29/2025; B24125-02-F 8/29/2025; B24125-02-G 8/29/2025; B24125-02-H 8/29/2025; B24125-03-A 8/29/2025; B24125-03-B 8/29/2025; B24125-03-C 8/29/2025; B24125-03-D 8/29/2025; B24125-03-E 8/29/2025; B24125-03-F 8/29/2025; B24125-03-G 8/29/2025; B24125-03-H 8/29/2025; B24125-04-A 8/29/2025; B24125-04-B 8/29/2025; B24125-04-C 8/29/2025; B24125-04-D 8/29/2025; B24125-04-E 8/29/2025; B24125-04-F 8/29/2025; B24125-04-G 8/29/2025; B24125-04-H 8/29/2025; B24125-05-A 8/29/2025; B24125-05-B 8/29/2025; B24125-05-C 8/29/2025; B24125-05-D 8/29/2025; B24125-05-E 8/29/2025; B24125-05-F 8/29/2025; B24125-05-G 8/29/2025; B24125-05-H 8/29/2025; B24125-06-A 8/29/2025; B24125-06-B 8/29/2025; B24125-06-C 8/29/2025; B24125-06-D 8/29/2025; B24125-06-E 8/29/2025; B24125-06-F 8/29/2025; B24125-06-G 8/29/2025; B24125-06-H 8/29/2025; B24125-07-A 8/29/2025; B24125-07-B 8/29/2025; B24125-07-C 8… (truncated, 15041 characters total — see the official FDA record for the full value)
Recalling firm:
California Dairies Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled April 8, 2026

Revitaderm Wound Care Gel, Benzalkonium Chloride 0.1%, packaged in 1.0 FL OZ (37 mL) bottle, shorter twist cap, Manufactured By: Blaine Labs, Inc. 11037 Lockport Place Santa Fe Springs, CA 90670, NDC 63347-120-02.

Microbial contamination of Non-Sterile Product: samples identified the presence of Lysinibacillus fusiformis and other Bacillus spp

ALL 50 STATES
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0692-2026
Lot/product code:
Lot#: BL3608, Exp. 07/01/28.
Recalling firm:
Blaine Labs Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled April 2, 2026

RAW FARM RAW CHEDDAR Original NEVER WARMED ABOVE 102F (TRULY RAW) MADE WITH WHOLE RAW MILK MADE IN USA KEEP REFRIGERATED INGREDIENTS: whole raw milk, vegetable rennet, cultures, kosher sea salt Produced By: RAW FARM, LLC www.rawfarmusa.com 8 oz (227g) UPC: 835204001177 16 oz (454g) UPC: 835204000156

Multi-state outbreak of E. coli O157:H7.

AZCACOFLGAILINMDNVTX
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-0762-2026
Lot/product code:
8 oz - BATCH: 20260212, BEST BY: 5/13/2026 and all prior batches/dates. 16 oz - BATCH: 20251027-4, BEST BY: 8/23/2026 and all prior batches/dates.
Recalling firm:
Raw Farm LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled April 2, 2026

RAW FARM SHREDDED RAW CHEDDAR 80 OZ [BULK ITEM] UPC: 835204000194

Multi-state outbreak of E. coli O157:H7.

AZCACOFLGAILINMDNVTX
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-0765-2026
Lot/product code:
80 oz - BATCH: 2026020, BEST BY: 5/6/2026 and all prior batches/dates.
Recalling firm:
Raw Farm LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled April 2, 2026

RAW FARM RAW CHEDDAR Jalapeno NEVER WARMED ABOVE 102F (TRULY RAW) MADE WITH WHOLE RAW MILK MADE IN USA KEEP REFRIGERATED INGREDIENTS: whole raw milk, vegetable rennet, cultures, kosher sea salt, 100% organic chili powder jalapeno, air dried green jalapeno peppers Produced By: RAW FARM, LLC www.rawfarmusa.com 8 oz (227g) UPC: 835204000330 16 oz (454g) UPC: 835204000354

Multi-state outbreak of E. coli O157:H7.

AZCACOFLGAILINMDNVTX
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-0763-2026
Lot/product code:
8 oz - BATCH: 20251128-2J, BEST BY: 9/24/2026 and all prior batches/dates. 16 oz - BATCH: 20251128-1J, BEST BY: 9/24/2026 and all prior batches/dates.
Recalling firm:
Raw Farm LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled April 2, 2026

RAW FARM RAW CHEDDAR SIMPLY SHREDDED Original MADE WITH: WHOLE RAW MILK TRULY RAW - NEVER WARMED ABOVE 102F MADE IN THE USA KEEP REFRIGERATED INGREDIENTS: WHOLE RAW MILK, VEGETABLE RENNET, CULTURES, KOSHER SEA SALT Produced By: RAW FARM, LLC www.rawfarmusa.com 8 oz (227g) UPC: 835204001184

Multi-state outbreak of E. coli O157:H7.

AZCACOFLGAILINMDNVTX
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-0764-2026
Lot/product code:
8 oz - BATCH: 20260212, BEST BY: 5/13/2026 and all prior batches/dates.
Recalling firm:
Raw Farm LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled April 2, 2026

RAW FARM ORIGINAL RAW CHEDDAR 80 OZ [BULK ITEM] UPC: 835204001160

Multi-state outbreak of E. coli O157:H7.

AZCACOFLGAILINMDNVTX
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-0766-2026
Lot/product code:
80 oz - BATCH: 20251015-4, BEST BY: 8/11/2026 and all prior batches/dates.
Recalling firm:
Raw Farm LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled March 21, 2026

Kian Pee Wan Capsules, 30-count bottles

Marketed Without an Approved NDA/ANDA: Product contains not listed on the label drug ingredients dexamethasone and cyproheptadine.

ALL 50 STATES
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0769-2026
Lot/product code:
All lots within expiry.
Recalling firm:
Buy-Herbal
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled March 18, 2026

Magnesium Sulfate in Water for Injection, 4g/100 mL (40mg/mL) IV bag, further packaged in cartons of 12 x 100 mL IV bags, Rx only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Ahmedabad, 382110, India, Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807, NDC 70121-1720-3.

Product mix up: a foil pouch labeled "Magnesium Sulfate in Water for Injection, 4 g/100 mL" actually contained an IV bag of Tranexamic Acid instead.

ALL 50 STATES
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0478-2026
Lot/product code:
Lot: AH250162, Exp 8/31/2027
Recalling firm:
Amneal Pharmaceuticals, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled March 11, 2026

Spray Dried Dairy Powder 25 kg bags or 1 metric ton totes

Salmonella spp. identified in finished product testing

ALL 50 STATES
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-0640-2026
Lot/product code:
NFDM Low Heat, NFDM High Heat, and SMP Medium Heat Lot Codes : 26015B; 26016B; 26017B; 26018B; 26019B; 26022B; 26023B; 26024B; 26024BT; 26025B; 26025BT; 26026B; 26027B; 26028B; 26029B; 26030B; 26034B; 26035B; 26040B; 26041B; 26041BT; 26042B; 26042BT; 26043B; 26044B; 26046BT; 26047BT; 26048BT. The products were packaged in 25 kg bags or 1 metric ton totes.
Recalling firm:
Lone Star Dairy Products LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled March 11, 2026

MILK-N-EGG MIX NET WEIGHT: 50 LBS, PROCESSED FROM NONFAT DRIED MILK, DRIED WHEY, DRIED EGG WHITES CONTAINS: EGG, MILK Mfred By: Griffith Goods, One Griffith Way, Stonecrest, GA

Potential Salmonella contamination. The firm was notified from their supplier that the nonfat dry milk may be contaminated with Salmonella.

AZCACOFLGAILLAMDMINCPASCTNTXWA
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-0693-2026
Lot/product code:
L 669896 Use By: 2-17-2027, L 669833 Use By: 2-16-2027, L 668712 Use By: 2-16-2027, L 668711 Use By: 2-16-2027, L 668710 Use By: 2-16-2027, L 668709 Use By: 2-16-2027 & L 668708 Use By: 2-16-2027.
Recalling firm:
Griffith Foods Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled March 11, 2026

MILK WASH NET WEIGHT: 50OZ (1417g) Packed Exclusively For: Chick-fil-A, Inc. 5200 Buffington Road Atlanta, GA 30349

Potential Salmonella contamination. The firm was notified from their supplier that the nonfat dry milk may be contaminated with Salmonella.

AZCACOFLGAILLAMDMINCPASCTNTXWA
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-0692-2026
Lot/product code:
L 671742 Best By AUG 30 2026, L 671741 Best By AUG 30 2026, L 670653 Best By AUG 24 2026, L 669617 Best By AUG 17 2026, L 669616 Best By AUG 17 2026, L 669611 Best By AUG 16 2026 & L 669610 Best By AUG 16 2026.
Recalling firm:
Griffith Foods Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled March 11, 2026

Costco Service Deli Department 63 MEATLOAF SEASONING MORE FLV Pack Size: 4-5lb. Bags Net Weight: 20lbs Allergy Information: CONTAINS: MILK, WHEAT Packed BY: Griffith Foods STONECREST, GA 30058

Potential Salmonella contamination. The firm was notified from their supplier that the nonfat dry milk may be contaminated with Salmonella.

AZCACOFLGAILLAMDMINCPASCTNTXWA
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-0691-2026
Lot/product code:
Lot 669648 Use By: 2-18-2027, Lot 669649 Use By: 2-18-2027, Lot 669650 Use By: 2-18-2027, Lot 669651 Use By: 2-19-2027, Lot 669652 Use By: 2-19-2027, Lot 669653 Use By: 2-19-2027, Lot 669654 Use By: 2-19-2027 & Lot 669655 Use By: 2-19-2027.
Recalling firm:
Griffith Foods Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled March 2, 2026

Webcol Alcohol Prep pad (70% isopropyl alcohol) 2 ply, 200 count boxes, Cardinal Health 200 LLC 3651 Birchwood Drive, Waukegan, IL 60085.

Non-Sterility: microbial contamination identified as Paenibacillus phoenicis

ALL 50 STATES
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0528-2026
Lot/product code:
Lot #: 25H065362; 25J013962; 25J034762; 25J064562; 25K004962; 25K041262; 25K065062; 25L015362; 25H065462; 25J014062; 25J035762; 25J064762; 25K005062; 25K041362; 25K065162; 25L015462; 25H066062; 25J014862; 25J035862; 25J064862; 25K006162; 25K041462; 25K065262; 25L015662; 25H066162; 25J014962; 25J035962; 25J064962; 25K006262; 25K041562; 25K065362; 25L016362; 25H066262; 25J033962; 25J050362; 25J065762; 25K006362; 25K041662; 25K064562; 25L015962; 25H066362; 25J034862; 25J050462; 25J066262; 25K005162; 25K040462; 25K064662; 25L016062; 25H066462; 25J034062; 25J050562; 25J066362; 25K006462; 25K040562; 25K065462; 25L030162; 25J013462; 25J034162; 25J050962; 25K004062; 25K019662; 25K040662; 25K065562; 25L058062; 25J013562; 25J034262; 25J051062; 25K004162; 25K020862; 25K040762; 25K065662; 25M022362; 25J014362; 25J034362; 25J051262; 25K005262; 25K020962; 25K040962; 25K066262; 25M028462; 25J014462; 25J034462; 25J051362; 25J065962; 25K019762; 25K041062; 25K066162; 25H065962; 25J034962; 25J051462; 25J065062; 25K019862; 25K041162; 25K064862; 25H065762; 25J035062; 25J051762; 25J065162; 25K021062; 25K041762; 25K065862; 25H065862; 25J035162; 25J051862; 25J066062; 25K021162; 25K041862; 25K079962; 25H066862; 25J035262; 25J051962; 25J066162; 25K021262; 25K041962; 25K080962; 25H066962; 25J035362; 25J075762;25K004262; 25K019962; 25K042162; 25K081062; 25J013162; 25J013662; 25J051162; 25K004362; 25K020062; 25K042262; 25K080062; 25J013262; 25J014562; 25J052062; 25K004462; 25K021362; 25K040862; 25K080162; 25J013362; 25J014662; 25J052162; 25K004562; 25K021462; 25K042062; 25K080262; 25J014162; 25J014762; 25J052262; 25K004662; 25K021562; 25K063862; 25K080362; 25J014262; 25J034562; 25J052362; 25K005362; 25K020162; 25K020562; 25K080462; 25H065562; 25J034662; 25J064362; 25K005462; 25K020262; 25K020362; 25K081162; 25H065662; 25J035462; 25J064462; 25K005562; 25K020662; 25K020462; 25K081262; 25H066562; 25J035562; 25J064662; 25K005662; 25K021662; 25K021962; 25K081362; 25H066662; 25J035662; 25J065262; 25K005762; 25K021762; 25K022062; 25K081462; 25H066762;25J050662; 25J065362; 25K004762; 25K021862; 25K063962; 25K081562; 25J012962; 25J050762; 25J065462; 25K004862; 25K040062; 25K064062; 25K080562; 25J013062; 25J050862; 25J065562; 25K005862; 25K040162; 25K064162; 25L014062; 25J013762; 25J051562; 25J065662; 25K005962; 25K040262; 25K064262; 25L014162; 25J013862; 25J051662; 25J065862; 25K006062; 25K040362; 25K064462; 25L015262 within Expiry
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenUndeclaredRecalled February 26, 2026

House of Flavors 4893 Chicago Vanilla Naturally Flavored Ice Cream, 3 GAL tub

Not listed on the label egg

IL
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-0621-2026
Lot/product code:
24059, 24130, 24207, 24342, 25105, 25120, 25134, 25206, 25254, 25301
Recalling firm:
House Of Flavors, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled February 13, 2026

Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 225mg 7-Hydroxymitragynine per container (7.5mg 7-OH per serving) LEMON DIETARY SUPPLEMENT Net Wt. 0.25 oz 30 TABLETS Supplement Facts 7-hydroxymitragynine 7.5 mg MANUFACTURED BY: Konig Products, LLC 30 N Gould Street, Suite R, Sheridan, WY 82801"; Packaging: White child-resistant plastic bottle with sticker label applied UPC 810057763779 (sometimes proceeded by 00)

A sample of the product revealed the active ingredient is in a quantity greater than the labeled specification.

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▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-1108-2026
Lot/product code:
B#AAW.501.3; all expiration dates
Recalling firm:
Shaman Botanicals, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 13, 2026

Rosabella brand MORINGA; DIETARY SUPPLEMENT CAPSULES; 60 capsules per bottle; Distributed by: Ambrosia Brands, LLC, 625 Randall Ave, St. 100, Cheyenne, WY 82001; SUGGESTED USE: As a dietary supplement, take two (2) veggie capsules once a day. For best results, take 20-30 min before a meal with an 8oz. glass of water or as directed by your health professional; UPC: 8 60012 16172 0

Product may be contaminated with Salmonella

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▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-0546-2026
Lot/product code:
Lot # - Expiration Date: 5020591 - 03/2027 5020592 - 03/2027 5020593 - 03/2027 5020594 - 03/2027 5020595 - 03/2027 5020596 - 03/2027 5030246 - 04/2027 5030247 - 04/2027 5030248 - 04/2027 5030249 - 04/2027 5030250 - 04/2027 5030251 - 04/2027 5040270 - 05/2027 5040271 - 05/2027 5040272 - 05/2027 5040273 - 05/2027 5040274 - 05/2027 5040275 - 05/2027 5040276 - 05/2027 5040277 - 05/2027 5040278 - 05/2027 5040279 - 05/2027 5050053 - 6/2027 5050054 - 6/2027 5050055 - 6/2027 5050056 - 6/2027 5060069 - 07/2027 5060070 - 07/2027 5060071 - 07/2027 5060072 - 07/2027 5060073 - 07/2027 5060074 - 07/2027 5060075 - 07/2027 5060076 - 07/2027 5060077 - 07/2027 5060078 - 07/2027 5060079 - 07/2027 5060080 - 07/2027 5080084 - 9/2027 5080085 - 9/2027 5080086 - 9/2027 5090107 - 10/2027 5090108 - 10/2027 5090109 - 10/2027 5090113 - 10/2027 5090114 - 10/2027 5090115 - 10/2027 5090116 - 10/2027 5090117 - 10/2027 5090118 - 10/2027 5100039 - 11/2027 5100048 - 11/2027
Recalling firm:
Ambrosia Brands LLC
Resolved:
August 13, 2026
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled February 13, 2026

Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 15mg 7-Hydroxymitragynine per container (7.5mg 7-OH per serving) LEMON DIETARY SUPPLEMENT Net Wt. 0.02 oz 2 TABLETS Supplement Facts 7-hydroxymitragynine 7.5 mg MANUFACTURED BY: Konig Products, LLC 30 N Gould Street, Suite R, Sheridan, WY 82801"; Packaging: Sealed silver metallic bag with a front and back sticker for the labels; Product label reads in part as "WHITE VEIN ADVANCED ALKALOIDS CHEWABLE TABLETS 150mg total 7-Hydroxymitragynine per container (10 Packets x 2 Tablets Each) 7.5mg 7-OH per tablet/serving, LEMON DIETARY SUPPLEMENT Net Wt. 0.17 oz 10 PACKETS 2 TABLETS EACH Supplement Facts 7-hydroxymitragynine 7.5 mg MANUFACTURED BY: Konig Products, LLC 30 N Gould Street, Suite R, Sheridan, WY 82801"; Packaging: Sealed black flexible plastic bag with multi color sticker label on front and back UPC 810057763724

A sample of the product had the active ingredient in a quantity greater than the labeled specification.

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The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-1107-2026
Lot/product code:
B#AAW.501.3; all expiration dates
Recalling firm:
Shaman Botanicals, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodUndeclaredRecalled January 28, 2026

Ashfiat Alharamain Energy Support 250ml/8fl. oz.

Not listed on the label tadalafil

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The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-1196-2026
Lot/product code:
Batch No: ENGOT24 EXP: OCT 2028 UPC: 1234561870003
Recalling firm:
AKKARCO LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled January 23, 2026

NAVITAS ORGANICS ORGANIC CHIA SEEDS NET WT 8 OZ (227g) INGREDIENTS: CERTIFIED ORGANIC CHIA SEED (SALVIA HISPANICA). Product of Mexico/Argentina/Paraguay. Distributed by Navitas Organics Novato, CA USA 94949 UPC: 858847000284

Potential contamination with Salmonella.

CACOCTFLGAIAILINKYMAMDMSNCNHNJNMNVNYOHORPATNTXVTWAWI
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-0533-2026
Lot/product code:
W31025283 - Best If Used By: End APR 2027 W31025286 - Best If Used By: End APR 2027 W31025287 - Best If Used By: End APR 2027 W31025311 - Best If Used By: End MAY 2027 W31025314 - Best If Used By: End MAY 2027 W31025315 - Best If Used By: End MAY 2027 W31025316 - Best If Used By: End MAY 2027 W31025317 - Best If Used By: End MAY 2027
Recalling firm:
Navitas, LLC.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled January 16, 2026

UDENYCA, pegfilgrastim-cbqv injection, 6 mg/0.6mL Single Dose Prefilled Syringe, Rx only, Manufactured by Accord BioPharma, Inc., 8041 Arco Corporate Drive, Suite 200, Raleigh, NC 27617, NDC 69448-025-63

Temperature Abuse. 116 cartons with specific serial numbers of Lot 2199821, were stored incorrectly in a controlled room temperature environment instead of the required refrigerated environment.

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The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0353-2026
Lot/product code:
Subset of Lot 2199821, Expires: 05/31/2027 Specific Serial Numbers being Recalled: 160R694TT06X; 1C74A686RPPG; 1W6A2M777N3V; 20825394KR8P; 242E2RK3EA92; 2DG49VH89EPG; 2WEA2ADK1P4H; 3KR2TVAG3VDH; 42M0V0G9PM84; 46E9XKDPTH1R; 4AM12WEAE48H; 4FGHR096DMNV; 4MWGWM991XNA; 4NEW8XD9DNM2; 4Y2PYDFN9YA1; 61EPX42R4K2A; 63FN9VW5CAV7; 69TG160DW2CV; 69XFP3TMTP7X; 6AWVDCNHTV61; 6CEFY72W5GPA; 6FHF1A59X0X4; 6GA64FNDVGXY; 6NW5FACPPWDW; 75V19CF2A0PA; 7HK7155YNAK3; 7R51VVA1WX9T; 7XCKXMH2EERC; 85D8MFVM66D4; 8F3Y5NFFHC64; 8RDWKPM53N5R; 8W1PVXC5NAFW; 9338DPED7P3R; 9A4CXFTGCPYN; 9FKN5NRDX99A; 9G79AR0RGAY4; 9K28G80GGYXN; 9NN7NXE40M13; A48PXEPE77YE; A8M168K58G64; AMR0RNWHTWMW; AR145NW8WTVX; AY19W6DEGRX4; C276HMDGRE49; CAY0ARAEGMCF; CKT370X2G4NP; D0DFAXCN6G5W; D54TXR8AD9Y8; DAK3XP1P3DMP; DH44AGKTX27F; E69E9K6C29VD; EK1D8P703RCH; EX947FYVW7Y6; F2K148YVNRDD; F4EVX8573F1V; FEXA7MENKWF1; FNDNMPAFH89D; G2W3WTMP5HK9; G5MN0F418FFY; G6XECANG6P01; G7FNVGWW3D72; GAHFFNX336GA; GKNTDP4AV6AA; GVPN5C4D23H6; GVPPYARK1FCD; GVXDAAA87GA1; GX7AP73W4HMH; HDTFT2W59K52; HDVG3W6VW59Y; HP703MKWGGM7; K8CGDV1301TP; KN6Y35T0A198; KVGC92YVC6XF; KYCP1Y7CK4R4; MEY2VW5MC0N9; MGH40F2679X3; N11XGETGDAVM; N9DGTY65NFGN; NH9VM1K2ECGP; NNCFT59RD1KF; NVFCXRWHX93N; P3XY0RNV0VPY; P609NH6W670V; P9Y7926YN82A; PA88CCXMWCMG; PKADTN18YR1X; PM0YHNNK6P4T; R11TYM5VE9CK; R45AXAEK4TTN; R6C3533P943P; RMW35MXX4R4K; RX75F9DA58W4; RXRCRP9272DG; RXTH041DMT5D; T2FW4C24F364; T442NHDFD7H8; TC3443DCR4F8; TK8TRR8NT92A; TT8K21TGYFWY; V255NE533X59; V6MYKEA7HN7P; V764DEYM4RYP; VCPTYV1EF0R1; VECGDTDV1Y3A; VEE09A07R9X5; VEER64AW2C51; VRN2TE3HPK5N; WF14WA03FNT2; WTP5TKRGNFGW; WWPMXV50FRM4; X1DKP0T2AE1W; X59C5AV3VDTG; XKG3T7811TD2; Y0CYY950EYK8; YCRW0EPK620Y; YNYA64T18DPW.
Recalling firm:
McKesson
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled January 15, 2026

a.) Live it Up brand Super Greens; Natural Wild Berry Flavor; Chlorella, Spirulina, Wheatgrass, Kale, Broccoli, Spinach, Barley grass, Moringa, Parsley; Whole food dietary supplement powder; 30 day supply; NET WT. 9.49oz (269.16g); Manufactured for Superfoods, Inc.; UPC: 860013190811 b.) Live it Up brand Super Greens; Natural Wild Berry Flavor; Chlorella, Spirulina, Wheatgrass, Kale, Broccoli, Spinach, Barley grass, Moringa, Parsley; Whole food dietary supplement powder; 30-0.32oz (9g) STICKS - NET WT. 9.52oz (270g); Manufactured for Superfoods, Inc.; UPC: 850077468070

Products may be contaminated with Salmonella Typhimurium

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▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-0434-2026
Lot/product code:
The lot code is printed on the bottom back of the packaging in black and begins with the letter "A". Expiration dates from 08/2026 to 01/2028. 2024 Lots: A24G012, A24I036, A24J005, A24J032, A24J037, A24K028, A24L014, A24L019, A24L032 2025 Lots: A25A005, A25A058, A25B006, A25D010, A25D036, A25D041, A25E008, A25F021, A25H009, A25H030, A25H045, A25I011, A25J036, A25K035 Stick Pack Products: 32925-1, 34525-1
Recalling firm:
SUPERFOODS, INC.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled January 15, 2026

Live it Up brand Super Greens; Chlorella, Spirulina, Wheatgrass, Kale, Broccoli, Spinach, Barley grass, Moringa, Parsley; Whole food dietary supplement powder; 30 day supply; NET WT. 8.5OZ (240G); Manufactured for Superfoods, Inc.; UPC: 860013190804 b.) Live it Up brand Super Greens; Chlorella, Spirulina, Wheatgrass, Kale, Broccoli, Spinach, Barley grass, Moringa, Parsley; Whole food dietary supplement powder; 30-0.28oz (8g) STICKS - NET WT. 8.47oz (240g); Manufactured for Superfoods, Inc.; UPC: 850077468063

Products may be contaminated with Salmonella Typhimurium

ALL 50 STATES
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-0433-2026
Lot/product code:
The lot code is printed on the bottom back of the packaging in black and begins with the letter "A". Expiration dates from 08/2026 to 01/2028. 2024 Lots: AA24H013, A24I019, A24J012, A24J041, A24K019, A24L001, A24L013, A24L036, A24L035 2025 Lots: A25A009, A25A017, A25A018, A25B005, A25B004, A25C018, A25C022, A25D021, A25E005, A25E007, A25F019, A25G033, A25F029, A25G065, A25H005, A25H012, A25I005, A25I010, A25I032, A25J005, A25J028, A25J037, A25K007, A25K013, A25L006 Stick Pack Products: 32825-1, 34425-1
Recalling firm:
SUPERFOODS, INC.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled January 9, 2026

Spring & Mulberry Lavender Rose Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a light blue box, UPC 850055470019, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individually or as a 3-pk, 6-pk, or 12-pk (Amazon only).

Potential Salmonella contamination

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The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-1099-2026
Lot/product code:
Product Number SMBARLR20001 Batch/Lot 025204 and Use By 01/31/2027 Batch/Lot 025205 and Use By 01/31/2027 Batch/Lot 025212 and Use By 02/28/2027 Batch/Lot 025216 and Use By 02/28/2027 Batch/Lot 025259 and Use By 03/31/2027 Batch/Lot 025260 and Use By 03/31/2027 Batch/Lot 026037 and Use By 08/31/2027 Batch/Lot 026040 and Use By 08/31/2027
Recalling firm:
Spring & Mulberry Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled January 9, 2026

Spring & Mulberry Blood Orange Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in an orange box, UPC 850055470200, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individually or as a 3-pk, 6-pk, or 12-pk (Amazon only).

Potential Salmonella contamination

ALL 50 STATES
▸Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
H-1106-2026
Lot/product code:
Product Number SMBARBO20001 Batch/Lot 025217 and Use By 02/28/2027 Batch/Lot 025289 and Use By 04/30/2027 Batch/Lot 025325 and Use By 05/31/2027
Recalling firm:
Spring & Mulberry Inc.
View official FDA record (opens in a new tab)