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Recalls affecting Wisconsin

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

Sure Unscented Anti-perspirant Deodorant Aerosol (Aluminum Chlorohydrate 10%), packaged in 6 oz (170 g) aerosol cans, Distributed by Idelle Labs, Ltd., El Paso, TX 79912, NDC 41595-5517-06

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-0208-2024
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
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)
Class IHigh risk
FoodBacteria/virusRecalled February 17, 2022

Abbott Similac 360 Total Care Infant Formula with Iron 20.6oz. and 30.3oz. palstic jar. 4 jars per case. 7oz. can. 6 cans per case. Item numbers: 68063 68065 68109 Retail UPCs: 070074680644 070074680668 070074681108

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-0943-2022
Lot/product code:
Batches: 33737SH00 33738SH00 33739SH00 35974SH00 35975SH00 36097SH00 36229SH01 32372SH00 32435SH00 32436SH00 36085SH00 36230SH00 37314SH00 32592K800 32595K800 35011K800 36138K800 36139K800 36231K800 36232K800 37291K800 37313K800
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 17, 2022

Abbott Similac For Spit Up Infant Formula with Iron 12.5oz. can. 6 cans per case. Item numbers: 5095976 Retail UPCs: 070074509600

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-0940-2022
Lot/product code:
Batches: 24447K807 24448K807 25674K800 25675K800 25677K800 25677K810 25798K800 26873K800 26874K800 26875K800 28024K800 28026K800 29247K800 29247K810 29248K800 29249K800 31502K800 31503K800 31504K800 33702K800 33703K800 33719K800 34854K800 34855K800 34856K800 34857K800 36100K800 36101K800 36102K800 36103K800
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 17, 2022

Abbott Similac Advance Step-2 22.5oz. plastic jar. 6 jars per case. Abbott Similac Advance 34oz. can. 6 cans per case. Abbott Similac Pro-Advance 20.6oz. and 859g. plastic jar. 6 jars per case. Item numbers: 6499113 6698313 6818113 6818313 Retail UPCs: 055325000808 055325001645 055325002864 055325002888

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-0925-2022
Lot/product code:
Batches: 27887SH00 31497SH00 35006SH00 23411SH00 25587SH00 26774SH00 27993SH00 28087SH00 29186SH00 30315SH00 31465SH00 31496SH00 35996SH00 36120SH10 36295SH10 32642SH00 35058SH10 35058SH00 36348SH00 37297SH00
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 17, 2022

Abbott Similac Alimentum with 2'-FL HMO, Abbott Similac Alimentum HMO, Abbott Alimentum HMO, Abbott Similac Alimentum infant formula, Abbott Similac Alimentum 400g can. 6 cans per case. Item numbers: 6749111 6749117 6749118 6749124 6749134 6749166 6749181 6749199 Retail UPCs: 070074124476 070074124438 0070074124490 070074124414 7703186029294 7501033958175 0070074122427 070074122441

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-0942-2022
Lot/product code:
Batches: 36146Z265 34768Z201 35014Z201 36146Z264 35014Z202 36146Z261 29284Z260 32416Z201 34768Z200 36146Z263 27938Z260 29284Z261 32416Z200 35014Z200 36146Z260 36146Z262 27938Z261 29284Z262 34768Z202
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 EleCare, EleCare LCP Hypoallergenic, Similac EleCare 400g. can. 6 cans per case. Item numbers: 5351034 5351066 5351039 5351077 Retail UPCs: 17703186031461 9340104000706 17501033957748 070074119281

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-0948-2022
Lot/product code:
Batches: 24549Z200 32429Z201 35025Z201 27871Z202 32429Z202 35025Z202 27871Z200 27871Z203 29258Z200 32429Z200 35025Z200 24549Z201 27871Z201 29258Z201 32429Z203
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)