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FDA food · drug · device recalls, merged

Before you eat it, take it, or plug it in — check.

Big Nope pulls three separate FDA recall feeds into one list per state, so you’re not searching three government databases to get one answer.

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)

Recalls nationwide

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

19,224 recalls found
NewestOldest
High riskLow riskAll
Wording
Class IHigh risk
FoodAllergenUndeclaredRecalled April 3, 2021

ISOMORPH 28 PURE WHEY iSOLATE CHOCOLATE MILKSHAKE DIETARY SUPPLEMENT NET WT. 2lb, UPC 6 49241 89876 4 & 5lb, UPC 6 49241 87830 8 jugs Manufactured By: APS Distribution, Inc. 6015-B Unity Drive Norcross, GA 30071

During an inspection by the FDA the firm was notified by FDA that the product contains not listed on the label milk, wheat & soy.

ALARAZCACOCTDEFLGAHIIAILINKYLAMAMDMEMIMOMSMTNCNDNENJNMNVNYOHOKORPARISCSDTNTXUTVAWAWIWVWY
▸Full report

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

Recall #:
F-0500-2021
Lot/product code:
2lb - All EXP DATES up to and including 04/2023 5lb - All EXP DATES up to and including 04/2023
Recalling firm:
Hi Tech Pharmaceuticals
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenUndeclaredRecalled April 3, 2021

ISOMORPH 28 PURE WHEY iSOLATE SMORES DIETARY SUPPLEMENT NET WT. 2lb, UPC 6 49241 89002 7 jugs Manufactured By: APS Distribution, Inc. 6015-B Unity Drive Norcross, GA 30071

During an inspection by the FDA the firm was notified by FDA that the product contains not listed on the label milk, wheat & soy.

ALARAZCACOCTDEFLGAHIIAILINKYLAMAMDMEMIMOMSMTNCNDNENJNMNVNYOHOKORPARISCSDTNTXUTVAWAWIWVWY
▸Full report

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

Recall #:
F-0505-2021
Lot/product code:
2lb - All EXP DATES up to and including 06/2023
Recalling firm:
Hi Tech Pharmaceuticals
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenUndeclaredRecalled April 3, 2021

ISOMORPH 28 PURE WHEY iSOLATE COOKIES N CREAM DIETARY SUPPLEMENT NET WT. 2lb, UPC 6 49241 89836 8 & 5lb, UPC 6 49241 87832 5 jugs Manufactured By: APS Distribution, Inc. 6015-B Unity Drive Norcross, GA 30071

During an inspection by the FDA the firm was notified by FDA that the product contains not listed on the label milk, wheat & soy.

ALARAZCACOCTDEFLGAHIIAILINKYLAMAMDMEMIMOMSMTNCNDNENJNMNVNYOHOKORPARISCSDTNTXUTVAWAWIWVWY
▸Full report

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

Recall #:
F-0502-2021
Lot/product code:
2lb - All EXP DATES up to and including 10/2023 5lb - All EXP DATES up to and including 09/2021
Recalling firm:
Hi Tech Pharmaceuticals
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenUndeclaredRecalled April 3, 2021

ISOMORPH 28 PURE WHEY iSOLATE VANILLA ICE CREAM DIETARY SUPPLEMENT NET WT. 5lb, UPC 6 49241 87837 7 jugs Manufactured By: APS Distribution, Inc. 6015-B Unity Drive Norcross, GA 30071

During an inspection by the FDA the firm was notified by FDA that the product contains not listed on the label milk, wheat & soy.

ALARAZCACOCTDEFLGAHIIAILINKYLAMAMDMEMIMOMSMTNCNDNENJNMNVNYOHOKORPARISCSDTNTXUTVAWAWIWVWY
▸Full report

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

Recall #:
F-0507-2021
Lot/product code:
5lb - All EXP DATES up to and including 11/2022
Recalling firm:
Hi Tech Pharmaceuticals
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenUndeclaredRecalled April 3, 2021

ISOMORPH 28 PURE WHEY iSOLATE VANILLA MILKSHAKE DIETARY SUPPLEMENT NET WT. 2LB, UPC 6 49241 89886 5 & 5lb, UPC 6 49241 87836 0 jugs Manufactured By: APS Distribution, Inc. 6015-B Unity Drive Norcross, GA 30071

During an inspection by the FDA the firm was notified by FDA that the product contains not listed on the label milk, wheat & soy.

ALARAZCACOCTDEFLGAHIIAILINKYLAMAMDMEMIMOMSMTNCNDNENJNMNVNYOHOKORPARISCSDTNTXUTVAWAWIWVWY
▸Full report

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

Recall #:
F-0508-2021
Lot/product code:
2lb - All EXP DATES up to and including 09/2023 5lb - All EXP DATES up to and including 12/2021
Recalling firm:
Hi Tech Pharmaceuticals
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenUndeclaredRecalled April 3, 2021

ISOMORPH 28 PURE WHEY iSOLATE STRAWBERRY MILKSHAKE DIETARY SUPPLEMENT NET WT. 2lb, UPC 6 49241 89866 5 & 5lb, UPC 6 49241 87835 3 jugs Manufactured By: APS Distribution, Inc. 6015-B Unity Drive Norcross, GA 30071

During an inspection by the FDA the firm was notified by FDA that the product contains not listed on the label milk, wheat & soy.

ALARAZCACOCTDEFLGAHIIAILINKYLAMAMDMEMIMOMSMTNCNDNENJNMNVNYOHOKORPARISCSDTNTXUTVAWAWIWVWY
▸Full report

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

Recall #:
F-0506-2021
Lot/product code:
2lb - All EXP DATES up to and including 11/2022 5lb - All EXP DATES up to and including 05/2021
Recalling firm:
Hi Tech Pharmaceuticals
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled April 8, 2021

Premium OrgaZEN 7000 capsule, 1-count per blister card, distributed by: Nutra Vita Co, Santa Fe Springs, CA, Made in USA , UPC 0 40232 32555 7

Marketed without an approved NDA/ANDA: Products found to contain not listed on the label sildenafil and/ or tadalafil

ALL 50 STATES
▸Full report

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

Recall #:
D-0641-2021
Lot/product code:
all lots
Recalling firm:
NSNY Distributor Inc
View official FDA record (opens in a new tab)
Class IHigh risk
DrugUndeclaredRecalled April 8, 2021

Ginseng Power 5000 capsule, 1- count per blister card, GS Natural Co, Los Angeles, CA 90010, UPC 0 40232 18144 3

Marketed without an approved NDA/ANDA: Products found to contain not listed on the label sildenafil and/ or tadalafil

ALL 50 STATES
▸Full report

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

Recall #:
D-0642-2021
Lot/product code:
all lots
Recalling firm:
NSNY Distributor Inc
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalRecalled May 12, 2021

MEDICALLY MINDED Hand Sanitizer Gel, ANTIMICROBIAL FORMULA, (Ethyl Alcohol 70% v/v), 8.5 FL OZ / 250 mL bottle, Made in Mexico, Distributed by SBL Brands, LLC Las Vegas, NV 89119. UPC: 6 76753 00359 1

Chemical Contamination: FDA analysis found 1 lot of MEDICALLY MINDED Hand Sanitizer Gel, ANTIMICROBIAL FORMULA (ethyl alcohol 70%) to be below the label claim for ethanol content and 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-0781-2021
Lot/product code:
Lot No: E082020, "Best Buy": 5/21/2022
Recalling firm:
Global Sanitizers LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalRecalled May 12, 2021

MEDICALLY MINDED Hand Sanitizer Gel, ANTIMICROBIAL FORMULA, (Ethyl Alcohol 70% v/v), 8 FL OZ (236 mL) bottle, Manufactured by Asiaticon, S.A. de C.V. Conkal 62, Jardines del Ajusco, Tlalpan, Ciudad de Mexico, C.P. 14200, Distributed by SBL Brands, LLC. Las Vegas, NV 89119. Made in Mexico UPC: 6 76753 00420 8,

Chemical Contamination: FDA analysis found 1 lot of MEDICALLY MINDED Hand Sanitizer Gel, ANTIMICROBIAL FORMULA (ethyl alcohol 70%) to be below the label claim for ethanol content and 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-0780-2021
Lot/product code:
Lot No: E082020, "Best Buy": 5/21/2022
Recalling firm:
Global Sanitizers LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled June 22, 2021

Limar Hand Sanitizer, Isopropyl Alcohol 70%, Cont. 4 oz bottles, Manufactured in Dominican Republic: by Ardil Comercial S.R.L., Santo Domingo, Dominican Republic UPC 7 487040 301587

Labeling Not Elsewhere Classified: Hand sanitizer packaged in containers resembling drinking water bottles.

ALL 50 STATES
▸Full report

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

Recall #:
D-0691-2021
Lot/product code:
Batch Number # 079932-4611-05-J, exp. date May 2022
Recalling firm:
Ardil Comercial S.R.L.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled July 14, 2021

Vy&Tea (Vietnamese Labeling with a green leaf and a bird underneath) 15/KLT 45.0G (15 tea sachets per box), Manufactured by Havyco No. 45, Group 1, National Highway 14, Son Hiep Hamlet, Tho Son Commune, Bu Dang District, Binh Phuoc Province, Vietnam, Website: trathaomocgiamcan.com.

Marketed Without An Approved NDA/ANDA: FDA analysis detected the presence of sibutramine.

ALL 50 STATES
▸Full report

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

Recall #:
D-0749-2021
Lot/product code:
Best By Date: 9/2021
Recalling firm:
Qikmoov LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalRecalled July 14, 2021

Neutrogena Beach Defense water+sun protection sunscreen spray BROAD SPECTRUM SPF 50, Avobenzone (3%), Homosalate (10%), Octisalate (5%), Octocrylene (10%), NET WT. 6.5 OZ. (184 g) aerosol can, Distributed by: JOHNSON & JOHNSON CONSUMER, INC. Skillman, NJ 08858, UPC 0 86800 11254 9

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-0844-2021
Lot/product code:
16621E01, exp 5/2024
Recalling firm:
Johnson & Johnson Consumer, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalRecalled July 14, 2021

Neutrogena Beach Defense water+sun protection sunscreen spray BROAD SPECTRUM SPF 60+, Avobenzone (3%), Homosalate (10%), Octisalate (5%), Octocrylene (10%) NET WT. 8.5 OZ. (240 g) aerosol can, Distributed by: JOHNSON & JOHNSON CONSUMER, INC. Skillman, NJ 08858, UPC 0 86800 11255 6

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-0845-2021
Lot/product code:
06320E26, exp 1/2023
Recalling firm:
Johnson & Johnson Consumer, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled July 16, 2021

ALPHA MALE+ Male Enhancer, fruit chew strips, 1 strip per foil pouch, Distributed by Umbrella Labs, Made in the USA, UPC 8 60003 03770 6. Also manufactured for and distributed by: Alpha Male Plus, Tucson, AZ UPC 8 60003 74518 2 (pouch), UPC 8 60003 74512 0(carton)

Marketed Without an Approved NDA/ANDA: FDA analysis determined the presence of tadalafil

ALL 50 STATES
▸Full report

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

Recall #:
D-0001-2022
Lot/product code:
All lots within expiry
Recalling firm:
Alpha-Tek LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled August 3, 2021

Lidocaine Hydrochloride Topical Solution, USP, 4% , 50 mL glass bottles, Rx Only, Teligent Pharma Inc. Buena, New Jersey 08310, NDC 52565-009-50.

Stronger than it should be Drug

ALL 50 STATES
▸Full report

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

Recall #:
D-0800-2021
Lot/product code:
Lot #:14218, Exp. Date 08/2022
Recalling firm:
Teligent Pharma, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled August 18, 2021

X RATED HONEY FOR MEN, packaged in 15g packets, 4 packets per box, UPC 6 13682 41232 2

Marketed without an approved NDA/ANDA: Product found to be tainted with Tadalafil.

ALL 50 STATES
▸Full report

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

Recall #:
D-0819-2021
Lot/product code:
All lots, Exp. 12/2025
Recalling firm:
Phe Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled September 15, 2021

KALE NET WT 16 OZ (1 LB) 454g Sold under the following brand names: Baker Farms 3667 Ellenton Norman Park Road, Norman Park GA 31771 UPC 8 13098 02001 6; Kroger DISTRIBUTED BY THE KROGER CO. CINCINNATI, OHIO 45202 UPC 0 11110 18170 1 & SEG Grocers DISTRIBUTED BY: SOUTHEASTERN GROCERS 8928 PROMINENCE PKWY #200, JACKSONVILLE, FL 32256 UPC 0 38259 11482 7

The firm was notified by one of their customers that during a random testing by ODA the product test positive for Listeria monocytogenes.

ALARFLGAKSMOMSNCNYOHVA
▸Full report

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

Recall #:
F-0009-2022
Lot/product code:
BEST BY 09-18-2021 107020-21832
Recalling firm:
Terry and Joe Baker Farms, Llc dba Baker Farms
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled October 12, 2021

Methocarbamol 500mg Tablet, packaged in a) #30 count (NDC 7133517952), b) #60 count (NDC 7133517954), and c) #90 count (NDC 7133517957) bottles, Rx only, Prinston Laboratories, Packaged by Bryant Ranch Prepack Burbank, CA 91504

Labeling: Label Error on Declared Strength; Bottles labeled as Methocarbamol 500 mg Tablets actually contain Methocarbamol 750 mg Tablets

ALL 50 STATES
▸Full report

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

Recall #:
D-0092-2022
Lot/product code:
Lot #: 163935, Exp: 10/31/2022
Recalling firm:
Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled November 17, 2021

Enoxaparin Sodium Injection, USP, 40 mg/0.4 mL, Single-Dose Syringes with Automatic Safety Device, For Subcutaneous Injection, Rx Only; 0.4 mL Syringes, Manufactured for Sandoz Inc., Princeton, NJ 08540, NDC 00781-3246-02; Carton (10 x 0.4 mL Syringes), Manufactured by Shenzhen Techdow Pharmaceutical Co., Ltd. Shenzhen City, Guangdong Province 518057, China for Sandoz Inc., Princeton, NJ 08540, NDC 00781-3246-64

Temperature Abuse; temperature excursion during shipping

ALL 50 STATES
▸Full report

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

Recall #:
D-0286-2022
Lot/product code:
Lot #SAB06761A, exp 04/2023
Recalling firm:
Sandoz Inc
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled November 19, 2021

AmericanScreening HAND SANITIZER (ethyl alcohol 70%) ANTIMICROBIAL FORMULA Vitamin E & Moisturizer, 8 FL OZ (237 mL) bottle with either a black or clear top, Distributed by American Screening LLC Shreveport, LA, 71106 UPC 8 40050 51579 2

Labeling Not Elsewhere Classified: Hand sanitizer packaged in containers resembling drinking water bottles.

ALL 50 STATES
▸Full report

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

Recall #:
D-0266-2022
Lot/product code:
Black capped bottles have no lot numbers but include expiration dates of 5/21/2022 and 05/24/2022. Clear capped bottles have neither lot numbers nor expiration dates.
Recalling firm:
American Screening LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled November 30, 2021

Lidocaine Hydrochloride, Topical Solution USP, 4% (40 mg/mL), packaged in 50 mL screw cap bottles, Rx Only, Manufactured by Teligent Pharma, Inc., Buena, NJ 08310, Distributed by: McKesson Corporation dba Sky Packaging, 4971 Southridge Blvd., Suite 101, Memphis, TN 38141, NDC 63739-997-64

Stronger than it should be Drug

ALL 50 STATES
▸Full report

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

Recall #:
D-0295-2022
Lot/product code:
Lot #: 16345, Exp. Date 01/2024
Recalling firm:
Teligent Pharma, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodAllergenUndeclaredRecalled December 17, 2021

Nature's Own Honey Wheat Bread, NET WT 20 oz (1LB 4 OZ) 567g, DISTRIBUTED BY FLOWERS BAKERIES, LLC THOMASVILLE, GA 31757 Single loaf UPC 0 72250 03706 8 & Double pack UPC 0 72250 00539 5

Not listed on the label milk

AZCACONMNVWY
▸Full report

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

Recall #:
F-0363-2022
Lot/product code:
BEST IF USED BY 12-26-21 Product Codes 128 346 03:00 through 128 346 05:00
Recalling firm:
Flowers Foods (Corporate Offices)
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalRecalled February 16, 2022

Sure Regular Antiperspirant Deodorant Aerosol (Aluminum Chlorohydrate 10%), packaged in 6 oz (170 g) aerosol cans, Distributed by Idelle Labs, Ltd., El Paso, TX 79912, NDC 41595-5518-06

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-0209-2024
Lot/product code:
All lots, expiry on or before August 2023
Recalling firm:
TCP HRB ACQUISITON LLC
View official FDA record (opens in a new tab)
Class IHigh risk
DrugChemicalRecalled February 16, 2022

Brut Classic Antiperspirant & Deodorant (aluminum chlorohydrate 20.9%) packaged in a) 4 oz. (113g) aerosol cans (UPC 00827755070085, NDC 41595-7103-1) and b) 6 oz. (170g) aerosol cans (UPC 00827755070108, NDC 41595-7103-2), Distributed by Idelle Labs, Ltd. El Paso, TX 79912 USA

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-0207-2024
Lot/product code:
All lots, expiry on or before August 2023
Recalling firm:
TCP HRB ACQUISITON LLC
View official FDA record (opens in a new tab)