BIGNOPE
Ko-fi

Recalls affecting Wisconsin

Data last updated: September 7, 2026 at 2:36 PM UTC

16,754 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 Mendietary 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 AliveMoringa 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. Braun0.9% 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 ValueOrganic 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

LipofitLipofit 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

KofinasGarlic 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 TemptationsChocolatey 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 SproutsRobust 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

MartinaMangoes

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)
Wording
Class IHigh risk
DrugUndeclaredRecalled April 26, 2023

NUX Male Enhancement capsule, 1-count blister card, distributed by SX Power CO., Chicago, Il 60612, UPC 6 01577 51236 3.

Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with not listed on the label sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.

ALL 50 STATES
Full report

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

Recall #:
D-0572-2023
Lot/product code:
Lot#: RO 927996, Exp: 12/25/2024
Recalling firm:
Gadget Island, Inc
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled April 26, 2023

DYNAMITE SUPER capsule, 58,000 MG, 1-count blister card, Made in America, UPC 6 75799 37602 7.

Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with not listed on the label sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.

ALL 50 STATES
Full report

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

Recall #:
D-0573-2023
Lot/product code:
Lot/Item#: OMS760-B, Exp: 12/2025
Recalling firm:
Gadget Island, Inc
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled March 13, 2023

Atovaquone Oral Suspension USP, 750 mg/5 mL, Packaged in 210 mL bottle, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, Manufactured by: Hetero Labs Limited, Jeedimetla, Hyderabad - 500 055, India, NDC# 31722-629-21.

Microbial Contamination of Non-Sterile Product: Objectionable organism, identified as Bacillus cereus, found in product during testing of repackaged product.

ALL 50 STATES
Full report

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

Recall #:
D-0567-2023
Lot/product code:
Lot# E220182, Exp. 12/31/2023
Recalling firm:
Camber Pharmaceuticals Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled February 24, 2023

Delsam Pharma's Artificial Eye Ointment (Mineral Oil 15%, White Petrolatum 83%), 3.5 grams (1/8 oz.) tube, Distributed By: Delsam Pharma Lic, Bronx, Newyork 10469, NDC 72570 122 35, UPC 3 72570 12235 3.

Non-Sterility: FDA analysis found unopened tubes to be contaminated with bacteria.

ALL 50 STATES
Full report

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

Recall #:
D-0488-2023
Lot/product code:
Batch # H29, Exp. Date 11/30/2023
Recalling firm:
Global Pharma Healthcare Private Limited
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled February 14, 2023

Purely Soothing 15% MSM Drops, packaged in a)15 ml, .5 fl oz bottle, UPC 7 31034 91382 9; and b) 30 ml, 1.014 fl oz bottle, UPC 7 31034 91379 9; Manufactured by: Pharmedica USA, Phoenix, AZ.

Non-Sterility

ALL 50 STATES
Full report

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

Recall #:
D-0456-2023
Lot/product code:
Lot #s: a) 1808051, Exp.: 01/01/2027; b) 2203PS01, Exp.: 01/01/2027
Recalling firm:
Pharmedica USA, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalRecalled February 14, 2023

Snowy Range Blue Alcohol Antiseptic 80% Topical Solution Hand Sanitizer Non-Sterile Solution, 4fl. oz. [118mL], Distributed by Reliable Products, LLC, Cheyenne, WY 82003, NDC 75288-100-04.

Chemical Contamination: FDA analysis found the product to contain methanol, acetaldehyde, and acetal above the limits.

ALL 50 STATES
Full report

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

Recall #:
D-0455-2023
Lot/product code:
All Lots
Recalling firm:
Nanomaterials Discovery Corporation
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled January 30, 2023

Artificial Tears (Carboxymethylcellulose Sodium) Lubricant Eye Drops, 10 MG in 1 ml, 1/2 fl oz (15 ml) bottle, Distributed by. EzriCare, LLC, Lakewood, NJ, NDC 79503-0101-15.

Non-Sterility: FDA analysis found unopened products to have bacterial contamination.

ALL 50 STATES
Full report

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

Recall #:
D-0919-2023
Lot/product code:
Lot #: PCMI005, Exp. date AUG-2024; PCMJ001, PCMJ002, PCMJ004, PCMJ005, PCMJ006, PCMJ008, PCMJ009, PCMJ010, PCMJ011, PCMJ012, PCMJ013, PCMJ014, PCMJ015, Exp. date MAR-2025
Recalling firm:
Global Pharma Healthcare Private Limited
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled January 30, 2023

Delsam Pharma's ARTIFICIAL TEARS (Carboxymethylcellulose Sodium) Lubricant Eye Drops, 10 MG in 1 ml, 1%, 1/2 fl oz (15 ml) bottle, Distributed By: Delsam Pharma Llc, Bronx, New York 10467, NDC 72570 121 15.

Non-Sterility: FDA analysis found unopened products to have bacterial contamination.

ALL 50 STATES
Full report

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

Recall #:
D-0921-2023
Lot/product code:
Lot #: PCMH001, PCMH002, PCMH005, PCMH007, Exp. date NOV-2023
Recalling firm:
Global Pharma Healthcare Private Limited
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalRecalled November 5, 2022

Adam's Polishes ALCOHOL BASED HAND SANITIZER, isopropyl alcohol 75% v/v, packaged in a) 4 fl. oz (118) spray bottle, NDC 74943-125-04; b) 8 fl. oz (237 mL) spray bottle, NDC 74943-125-08; c) 1 PINT / 16 fl. oz (475 ml.) spray bottle, NDC 74943-125-16; and d) 1 GALLON / 128 fl. oz. (3,785 ml.) jug, NDC 74943-125-28, Manufactured by B&B Blending, LLC, Northglenn, CO.

Chemical Contamination: FDA analysis found 1 lot of Adam's Polishes ALCOHOL BASED HAND SANITIZER isopropyl alcohol 75% v/v to contain methanol.

ALL 50 STATES
Full report

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

Recall #:
D-0066-2023
Lot/product code:
Lot: 133475
Recalling firm:
Adam's Polishes LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenUndeclaredRecalled October 20, 2022

Umami Everyday Savory Spice, 5 fl. oz. (148 mL) glass bottle, UPC 8-50000-72724-3, Co-Packed with Seed Ranch Flavor Co., Denver, CO 80216 Ambient storage - minimum 35 degrees, maximum 85 degrees.

Three sauces contain not listed on the label soy.

ALL 50 STATES
Full report

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

Recall #:
F-0175-2023
Lot/product code:
Lot Codes: 120122 062521
Recalling firm:
Seed Ranch Flavor Co
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenUndeclaredRecalled October 20, 2022

Everything But The Sushi & Dumplings, 5 fl. oz. (148 mL) glass bottle, UPC 8-60008-58851-7, Made for Seed Ranch Flavor Co., LLC Boulder, CO 80302. Ambient storage - minimum 35 degrees, maximum 85 degrees.

Three sauces contain not listed on the label soy.

ALL 50 STATES
Full report

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

Recall #:
F-0176-2023
Lot/product code:
Lot Codes: 071122 081822 6188 BB061025
Recalling firm:
Seed Ranch Flavor Co
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenUndeclaredRecalled October 20, 2022

Umami Everyday Sauce, 5 fl. oz. (148 mL) glass bottle, UPC 8-67732-00032-2, Made for Seed Ranch Flavor Co., LLC, Boulder, CO 80302 Ambient storage - minimum 35 degrees, maximum 85 degrees.

Three sauces contain not listed on the label soy.

ALL 50 STATES
Full report

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

Recall #:
F-0174-2023
Lot/product code:
Lot Codes: 010821 020921 030821 051721 081821 120321 012022 031422 042522 081822 092022
Recalling firm:
Seed Ranch Flavor Co
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled May 24, 2022

Artri King Reforzado con Ortiga Omega 3 Tablets, ORIGINAL, 100-count bottles, Melchor Ocampo No. 55 Local D, Delegacion Xochimilco, C.P. 16800, Mexico, D.F., UPC 7 501031 111190.

Marketed Without An Unapproved NDA/ANDA: Product lot found to be tainted with not listed on the label diclofenac, an FDA approved nonsteroidal anti-inflammatory drug (NSAID) for the treatment of pain and inflammation.

ALL 50 STATES
Full report

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

Recall #:
D-1157-2022
Lot/product code:
Lot: LTARTKNGOMG30720, Exp Diciembre 2026
Recalling firm:
Walmart Inc
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalRecalled March 30, 2022

Suave 24-Hour Protection Aerosol Antiperspirant Powder scent, Aluminum Chlorohydrate (19.1%), packaged in a) 4 oz. cans (UPC 0 79400 75150 8), and b) 6 oz. cans (UPC 0 79400 78490 2), Dist. By Unilever, Trumbull, CT 06611

Chemical contamination: presence of benzene

ALL 50 STATES
Full report

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

Recall #:
D-0210-2024
Lot/product code:
all lots, expiry 9/30/2023
Recalling firm:
Unilever United States Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled March 4, 2022

SyrSpend SF Suspending Base, Cherry Flavored, packaged in a) 500mL bottles (NDC 51552-1123-5) and b) 4L bottles (NDC 51552-1123-9), Rx Only, Manufactured for Fagron, Inc., St. Paul, MN 55120.

Microbial Contamination of Non-Sterile Product: Product is contaminated with Burkholderia gladioli.

ALL 50 STATES
Full report

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

Recall #:
D-0856-2022
Lot/product code:
Lot #: a) A67185, Exp. Date 08/31/2024; b) Lot #: A67186, Exp. Date 08/31/2024
Recalling firm:
Fagron, Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 17, 2022

Abbott EleCare Jr Amino Acid-Based Nutrition Powder Unflavored 14.1oz. can. 6 cans per case. Item numbers: 55253 Retail UPCs: 070074552545 70074552545

Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced

ALL 50 STATES
Full report

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

Recall #:
F-0951-2022
Lot/product code:
Batches: 23441Z200 25715Z200 26723Z200 26724Z200 26858Z200 27923Z200 27924Z200 27932Z200 27934Z200 29265Z200 30390Z200 30407Z200 31408Z200 34013Z200 34774Z200 35024Z200 35029Z200 36153Z200
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 17, 2022

Abbott Infant Formula Powder 12.6oz. can. 6 cans per case. Item numbers: Clinical Retail UPCs: N/A - Clinical

Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced

ALL 50 STATES
Full report

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

Recall #:
F-0957-2022
Lot/product code:
Batches: 29169K800
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 17, 2022

Abbott Similac 360 Total Care Sensitive Infant Formula with Iron 7oz. can. 6 cans per case. 20.1oz. and 29.5oz. plastic jar. 4 jars per case. Item numbers: 68070 68072 68118 Retail UPCs: 070074680712 070074680736 070074681191

Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced

ALL 50 STATES
Full report

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

Recall #:
F-0947-2022
Lot/product code:
Batches: 30349SH00 30351SH00 30353SH00 32461SH00 36095SH00 34955SH00 34956SH00 34956SH01 34957SH00 36217SH00 32355K800 32464K800 35076K800 35077K800 36136K800 36137K800
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 17, 2022

Abbott Similac Sensitive 34oz. plastic jar. 6 jars per case. Abbott Similac Sensitive Infant Formula with Iron 12.5oz. can and 20.1oz. plastic jar. 6 units per case. Item numbers: 68082 5753978 6748901 674891L Retail UPCs: 070074680835 070074575414 070074122380

Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced

ALL 50 STATES
Full report

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

Recall #:
F-0938-2022
Lot/product code:
Batches: 28015SH00 28013SH00 28016SH00 28018SH00 28019SH00 30302SH00 30447SH00 30449SH00 32610SH00 36214SH00 36215SH00 23390K800 23392K800 23422K800 23423K800 23424K800 23425K800 23428K800 23429K800 24454K800 24455K800 24483K800 24484K800 24485K800 24486K800 24487K800 24488K800 24504K800 24505K800 24506K800 24517K800 25591K800 25592K800 25678K800 25678K801 25679K800 25734K800 25735K800 26741K800 26743K800 26745K800 26788K800 26789K800 27879K800 27892K800 27893K800 27947K800 27948K800 27949K800 27950K800 27952K800 28020K800 28021K800 28022K800 28099K800 28100K800 28101K800 28142K800 28143K800 28144K800 28145K800 28146K800 29191K800 29192K800 29193K800 29194K800 29195K800 29234K800 29235K800 29236K800 29293K800 29294K800 30300K800 30301K800 30322K800 30323K800 30338K800 30339K800 30356K800 30357K800 30358K800 30360K800 30361K800 30444K800 30446K800 30448K800 30450K800 30451K800 30452K800 31471K800 31472K800 31473K800 31474K800 32619K800 32620K800 32627K800 32628K800 32629K800 32630K800 32631K800 32632K800 32633K800 32680K800 32681K800 32682K800 33705K800 33709K800 33710K800 33711K800 33712K800 33713K800 33714K800 33715K800 33724K800 33735K800 33830K800 33831K800 34850K800 34850K801 34851K800 34858K810 34859K810 34862K800 34871K800 34872K800 34873K800 34874K800 34945K800 34946K800 34947K800 34948K800 34949K800 34950K800 35051K800 35052K800 35074K800 35075K800 35197K800 35976K800 35977K800 35978K800 36091K800 36093K800 36094K800 36096K800 36128K800 36129K800 36130K800 36131K800 36132K800 36133K800 37279K800 37279K801 37280K800 37281K800 37282K800 37322K800 37428K800 37429K800 25682SH00 27878SH00 28090SH00 29205SH00 29244SH00 31501SH00 32615SH00 32617SH00 34807SH00 34851SH00 36116SH00 26839SH00
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 17, 2022

Abbott Similac Organic 7oz. can. 6 cans per case. Abbott Similac Organic with A2 Milk Infant Formula with Iron 20.6oz. plastic jar. 4 jars per case. 23.2oz plastic jar. 6 jars per case. Item numbers: 68013 68092 5082178 Retail UPCs: 070074680156 070074680934 070074508221

Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced

ALL 50 STATES
Full report

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

Recall #:
F-0945-2022
Lot/product code:
Batches: 24397K800 27994SH00 27995SH00 24400SH00
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 17, 2022

Abbott Similac Advance Infant Formula with Iron 12.4oz. can, 23.2oz. plastic jar, 20.6oz. plastic jar. 6 units per case. Abbott Similac Pro-Advance 34oz. plastic jar. 6 jars per case. Item numbers: 53359 68084 5595776 6748701 Retail UPCs: 070074533605 070074680859 070074559582 070074122373

Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced

ALL 50 STATES
Full report

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

Recall #:
F-0935-2022
Lot/product code:
Batches: 23432SH00 23433SH00 24461SH00 24462SH00 25593SH00 25594SH00 25596SH00 26765SH00 26766SH00 26795SH00 26796SH00 27001SH00 27003SH00 27996SH00 27997SH00 27998SH00 28025SH00 28111SH00 29229SH00 29230SH00 30359SH00 31585SH00 31587SH00 31588SH00 35059SH00 35072SH00 37245SH00 23403K800 23404K800 23406K800 23408K800 23410K800 23434K800 23435K800 23436K800 23437K800 24473K800 24474K800 24475K800 24476K800 24477K800 24478K800 24491K800 24492K800 24512K800 24513K800 24514K800 24518K800 24519K800 24520K800 24521K800 24522K800 25578K800 25580K800 25581K800 25582K800 25583K800 25584K800 25585K800 25597K800 25599K800 25601K800 25602K800 25603K800 25666K800 25669K800 25670K800 25671K800 25672K800 25680K800 25696K800 25697K800 25698K800 25699K800 26751K800 26753K800 26754K800 26755K800 26757K800 26757K801 26758K800 26775K800 26776K800 26792K800 26793K800 26794K800 26844K800 26845K800 26846K800 26847K800 26848K800 26849K800 26850K800 26851K800 27002K800 27894K800 27895K800 27896K800 27897K800 27898K800 27899K800 27900K800 27901K800 27902K800 27903K800 27904K800 27905K800 27906K800 27907K800 27908K800 27909K800 27962K800 27963K800 27964K800 27965K800 27966K800 27967K800 27968K800 27969K800 27969K810 27970K800 27999K800 28004K800 28005K800 28006K800 28007K800 28009K800 28011K800 28028K800 28030K800 28084K800 28085K800 28093K800 28094K800 28095K800 28107K800 28108K800 28109K800 28110K800 28112K800 28113K800 28114K800 28115K800 28116K800 28149K800 28150K800 28151K800 29196K800 29197K800 29198K800 29199K800 29200K800 29207K800 29208K800 29221K800 29223K800 29224K800 29227K800 29250K800 29251K800 29252K800 29253K800 29254K800 29255K800 29256K800 29257K800 30310K800 30324K800 30346K800 30347K800 30348K800 30350K800 30352K800 30354K800 30366K800 30367K800 30368K800 30370K800 30371K800 30373K800 31477K800 31479K800 31485K800 31487K800 31489K800 31491K800 31505K800 31506K800 32596K800 32621K800 32622K800 32623K800 32634K800 32635K800 32637K800 32678K800 32679K800 33786K800 33787K800 33788K800 33789K800 33790K800 33791K800 33832K800 33833K800 34793K800 34795K800 34797K800 34811K800 34813K800 34814K800 34816K800 34817K800 34818K800 34819K800 34820K800 34852K810 34853K810 34863K800 34864K800 34875K800 34876K800 34877K800 34878K800 34879K800 34880K800 34881K800 34882K800 34883K800 34936K800 34937K800 34938K800 34939K800 34941K800 34942K800 34951K800 34952K800 34953K800 34954K800 35070K800 35071K800 35984K800 35985K800 35986K800 36087K800 36140K800 36141K800 36142K800 36143K800 36225K800 36226K800 36227K800 36228K800 37242K800 37243K800 32640SH00 23405SH00 23405SH01 24527SH00 24569SH00 25693SH00 26836SH00 27880SH00 28147SH00 28148SH00 29183SH00 29184SH00 32593SH00 37246SH00 37247SH00 37248SH00 37249SH00 37250SH00 37309SH00 37310SH00
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 17, 2022

Abbott EleCare Jr Amino Acid-Based Nutrition Powder Chocolate 14.1oz. can. 6 cans per case. Item numbers: 66273 Retail UPCs: 070074662718

Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced

ALL 50 STATES
Full report

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

Recall #:
F-0953-2022
Lot/product code:
Batches: 24532Z200 28129Z200 30400Z200 34935Z200 36154Z200
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 17, 2022

Abbott Similac Total Comfort Infant Formula with Iron 12.6oz. can. 6 cans per case. Item numbers: 62599 Retail UPCs: 070074626000

Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced

ALL 50 STATES
Full report

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

Recall #:
F-0939-2022
Lot/product code:
Batches: 24449K800 24449K801 24450K800 24482K800 24515K800 24516K800 24566K800 24566K801 25571K800 25571K801 25650K800 25651K800 25687K800 25688K800 26747K800 26748K800 26817K800 26818K800 26819K800 26830K800 26832K800 26834K800 26835K800 27888K800 27889K800 27890K800 27891K800 27951K800 28017K800 28086K800 28088K800 28098K800 28178K800 28179K800 28179K801 28180K800 29219K800 29220K801 29237K800 29238K800 30314K800 30316K800 30317K800 31467K800 31468K800 31469K800 31470K800 31584K800 31586K800 32609K800 32611K800 32612K800 33706K800 33706K801 33707K800 33708K800 34073K800 34800K800 34801K800 34844K800 34844K801 34845K800 34846K800 34847K800 34865K800 34866K800 34867K800 34868K800 34869K800 34870K800 34943K800 34944K800 35981K800 35982K800 35983K800 36086K800 36121K800 36122K800 36212K800 36213K800 37238K800 37239K800 37240K800 37241K800 37298K800 37299K800 37300K800 37301K800 37302K800 37430K800 37431K800
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 17, 2022

Abbott Similac Organic with A2 Milk Toddler Drink 23.2oz plastic jar. 4 jars per case. Abbott Similac Organic Toddler with A2 Milk Infant Formula with Iron 20.6oz. plastic jar. 4 jars per case. Item numbers: 67905 68104 Retail UPCs: 070074677576 070074681054

Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced

ALL 50 STATES
Full report

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

Recall #:
F-0944-2022
Lot/product code:
Batches: 24399SH00 33780SH00
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 17, 2022

Abbott Similac Alimentum Eye Q Plus 400g. can. Abbott Alimentum Eye Q 400g. can. Abbott Alimentum Eye Q Hypoallergenic 400g. can. 6 cans per case. Item numbers: 6208407 6208418 6208481 6208482 6208483 Retail UPCs: 070074110431 070074123905 070074110356 070074111834 070074110271

Consumer complaints related to Cronobacter sakazakii or Salmonella Newport in infants and evidence of Cronobacter sakazakii in the manufacturing facility where the product had been produced

ALL 50 STATES
Full report

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

Recall #:
F-0956-2022
Lot/product code:
Batches: 26812Z261 29209Z201 30285Z263 32412Z222 33690Z201 26812Z262 27939Z263 29209Z203 30285Z262 32412Z223 26812Z263 27939Z260 29209Z200 30285Z260 32412Z220 32648Z200 26812Z260 27939Z261 29209Z202 30285Z261 32412Z221 33690Z200 33690Z210 27939Z262 29209Z204 30285Z264 32412Z224 33690Z202
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)