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Recalls affecting District of Columbia

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

16,076 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
FoodBacteria/virusRecalled February 17, 2022

Abbott EleCare Infant Formula Unflavoured 400g can. 6 cans per case. Item number 5466539 Retail unit UPC 070074104591

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-0918-2022
Lot/product code:
Batch 26811Z200
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 17, 2022

Abbott Similac Human Milk Fortifier 0.9g Pouch / Sachet, 50 Pouch / Sachet per retail unit. 3 retail units per case Item numbers: 54598 5459813 5459814 5459820 5459886 6771009 Retail UPCs: 70074545998 070074545998 055325545996 070074109404 070074103297 070074671833

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-0919-2022
Lot/product code:
Batches: 22349Z200 25609Z200 26914Z200 26915Z200 26916Z200 26917Z200 26918Z200 26919Z200 26920Z200 26921Z200 27073Z200 28077Z200 28158Z200 28162Z200 28166Z200 29385Z200 30512Z200 30513Z200 30521Z200 31525Z200 31533Z200 31534Z200 31543Z200 32649Z200 32655Z200 32656Z200 32660Z200 32660Z210 32671Z200 33751Z200 33752Z200 34045Z200 34046Z210 34892Z200 34901Z200 35112Z200 35113Z200 35163Z200 36170Z200 30522Z200 32657Z200 22353Z200 22354Z200 26782Z200 26785Z200 27982Z200 27983Z200 31541Z200 33753Z200 34890Z200 34891Z200 35164Z200 36171Z200 24472Z200 25610Z200 27984Z200 32672Z200 32673Z200 32674Z200 22296Z200 22297Z200 25712Z200 26781Z200 26786Z200 26787Z200 30514Z200 30523Z200 31524Z200 31532Z200 31542Z200 32658Z200 33659Z200 33756Z200 33757Z200 34889Z200 36169Z200 22350Z200 22351Z200 22352Z200 22355Z200 22356Z200 22357Z200 23358Z200 23359Z200 24465Z200 24466Z200 24467Z200 24468Z200 24469Z200 24470Z200 24471Z200 25605Z200 25606Z200 25607Z200 25608Z200 25611Z200 25612Z200 25613Z200 25614Z200 25705Z200 25706Z200 25707Z200 25708Z200 25709Z200 25710Z200 25711Z200 25713Z200 25714Z200 26772Z200 26777Z200 26778Z200 26779Z200 26783Z200 26784Z200 26852Z200 26853Z200 27074Z200 27854Z200 27855Z200 27856Z200 27857Z200 27985Z200 27986Z200 28075Z200 28078Z200 28079Z200 28080Z200 28159Z200 28160Z200 28161Z200 28163Z200 28164Z200 28165Z200 30515Z200 30516Z200 30519Z200 30520Z200 31526Z200 31527Z200 31528Z200 31529Z200 31530Z200 31531Z200 31535Z200 31536Z200 31537Z200 31538Z200 31539Z200 31540Z200 32650Z200 32651Z200 32652Z200 32653Z200 32654Z200 32675Z200 33661Z200 33743Z200 33744Z200 33745Z200 33746Z200 33747Z200 33748Z200 33749Z200 33750Z200 33754Z200 33755Z200 33885Z200 33886Z200 34043Z200 34044Z200 34887Z200 34888Z200 34893Z200 34894Z200 34895Z200 34896Z200 34897Z200 34898Z200 34899Z200 34900Z200 34902Z200 34903Z200 34904Z200 34905Z200 35110Z200 35111Z200 28076Z200
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 17, 2022

Abbott Similac Pro-Advance Infant Formula with Iron 20.6oz. and 23.2oz. plastic jar. 4 jars per case; 34oz. plastic jar. 6 jars per case; 7oz. can. 6 cans per case. Item numbers: 66081 66655 67922 68088 Retail UPCs: 070074660806 070074666563 070074679167 070074680897

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-0931-2022
Lot/product code:
Batches: 23407SH00 23409SH00 24460SH00 24480SH00 24523SH00 24524SH00 25598SH00 25600SH00 25694SH00 25695SH00 25736SH00 25780SH00 26762SH00 26764SH00 26831SH00 26833SH00 27886SH10 23375SH00 23376SH00 23430SH00 23431SH00 24456SH00 24457SH00 24458SH00 24459SH00 24490SH00 24526SH00 24615Sh00 24615SH10 25570SH00 25586SH00 25652SH00 25653SH00 26749SH00 26750SH00 26752SH00 26759SH00 26761SH00 26824SH00 26825SH00 26826SH00 26827SH00 26828SH00 26829SH00 26841SH00 26843SH00 27881SH00 27882SH00 27883SH00 27884SH00 29181SH00 29182SH00 29225SH00 29226SH00 29228SH00 29295SH00 29296SH00 29297SH00 30308SH00 31457SH00 31459SH00 31460SH00 31462SH00 31483SH00 31484SH00 31486SH10 31488SH00 31490SH00 31492SH00 31493SH10 31493SH11 31494SH00 31550SH00 31551SH00 31577SH00 31578SH00 32616SH00 32618SH00 32668SH00 32669SH00 32670SH00 33736SH00 34798SH00 34960SH00 34961SH00 35039SH00 35040SH00 35041SH00 35042SH00 35198SH00 35962SH00 35963SH00 35964SH00 35965SH00 35966SH00 35967SH00 35968SH00 35969SH00 35970SH00 35971SH00 35972SH00 35973SH00 36189SH00 36190SH00 36191SH00 36193SH00 36194SH00 36195SH00 36196SH00 36219SH00 36220SH00 36221SH00 36222SH00 36223SH00 36224SH00 23401K800 23402K800 24479K800 25595K800 26842K800 27886K800 27957K800 27958K800 27959K800 27960K800 28012K800 28092K800 28103K800 28106K800 29185K800 30325K800 30326K800 30441K800 30441K810 30442K800 33717K800 33718K800 33779K800 33782K800 27974SH00 27975SH00 27976SH00 27991SH00 28008SH00 28010SH00 28104SH00 28105SH00 28156SH00 28157SH00 29206SH00 29222SH00 30305SH00 30306SH00 30307SH00 30340SH00 30341SH00 30342SH00 30362SH00 30363SH00 30369SH00 31481SH00 31482SH00 31573SH00 31575SH00 31576SH00 32590SH00 32591SH00 34810SH00 34812SH00 34812SH10 35060SH00 35061SH00 35082SH00 35082SH01 35083SH00 35084SH00 35990SH00 35991SH00 36134SH00 36135SH00 37292SH00 37293SH00
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 17, 2022

Abbott Similac Pro-Total Comfort Infant Formula with Iron 20.1oz. and 22.5oz. plastic jar. 4 jars per case. 34oz. plastic jar. 6 jars per case. 7oz. can. 6 cans per case. Item numbers: 66798 66939 67925 68107 Retail UPCs: 070074667997 070074669403 070074679266 070074681085

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-0934-2022
Lot/product code:
Batches: 26838SH00 26860SH00 26861SH00 30318SH00 31498SH00 31580SH00 33730SH00 24451SH00 24565SH00 26738SH00 26791SH00 23495K800 24481K800 25572K800 25588K800 26739K800 26837K800 28014K800 28141K800 28152K800 29243K800 29246K800 30319K800 31466K800 31579K800 31581K800 32613K800 32614K800 34860K800 36123K800 37236K800 27977SH00 27978SH00 27990SH00 28096SH00 28097SH00 30303SH00 30304SH00 31582SH00 31583SH00 33726SH00 33727SH00 33728SH00 33729SH00 37237SH00 37303SH00
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 17, 2022

Abbott Similac Sensitive Infant Formula with Iron 22.5oz. plastic jar. 6 jars per case. Item numbers: 5081776 Retail UPCs: 070074508184

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-0937-2022
Lot/product code:
Batches: 23426SH00 23427SH00 25577SH00 25579SH00 25665SH00 25681SH00 26840SH00
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 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 Similac Alimentum Toddler Drink 12.1oz. can. 6 cans per case. Item numbers: 68398 Retail UPCs: 070074683997

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-0920-2022
Lot/product code:
Batches: 31552Z200
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 Similac Pro-Advance 23oz. and 34oz. plastic jar. 6 jars per case. Item numbers: 6720413 6721313 Retail UPCs: 055325002567 055325002581

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-0932-2022
Lot/product code:
Batches: 30343SH00 34959SH00 24494SH00 30343SH01 32594SH00 32594SH10 32594SH20 34799SH00 34959SH01
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 17, 2022

Abbott EleCare Amino Acid-Based Powder Infant Formula with Iron 14.1oz. can, Abbott Elecare 400g. can, Abbott Elecare Unflavored 14.1oz. can. 6 cans per case. Item numbers: 55251 5525157 5525189 Retail UPCs: 070074535111 070074116297 070074119854

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-0949-2022
Lot/product code:
Batches: 22331Z200 23377Z200 23438Z200 23439Z200 25562Z200 25562Z220 25563Z200 25729Z200 25730Z200 26731Z200 27922Z200 27931Z200 28124Z200 28125Z200 28126Z200 30291Z200 30292Z200 30517Z200 30518Z200 31392Z200 31402Z200 32421Z200 32684Z200 33694Z200 33695Z200 34012Z200 34769Z200 34770Z200 34771Z200 34771Z210 35023Z200 35032Z200 36149Z200 36150Z200 36151Z200 22331Z202 22331Z201
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 17, 2022

Abbott Similac EleCare HMO, Abbott Similac EleCare, Abbott EleCare Similac Gold, Abbott EleCare Similac 400g can. 6 cans per case Item numbers: 6676006 6676012 6676021 6676025 6676030 6676045 6676053 6676057 Retail UPCs: 8699548995217 0070074124155 0070074123851 0070074120195 070074120850 070074122502 0070074120157

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-0929-2022
Lot/product code:
Batches: 25557Z200 27930Z200 28130Z201 29266Z200 30374Z200 30384Z201 32422Z201 33693Z200 36144Z202 25557Z201 30384Z202 33693Z202 34767Z201 35031Z202 36144Z205 27930Z202 36144Z203 25557Z203 30374Z202 36144Z204 34767Z202 25557Z205 28130Z200 29266Z201 30384Z200 32422Z202 33693Z201 35031Z201 36144Z200 25557Z204 28130Z202 30374Z201 32422Z210 34767Z200 35031Z200 36144Z201 25557Z202 27930Z201 28130Z203
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 17, 2022

Abbott Similac PM 60/40 Low Iron Infant Formula, 14.1oz. can. 6 cans per case. Item numbers: 00850 Retail UPCs: 070074608501

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-0958-2022
Lot/product code:
Batches: 27032K80 (can) / 27032K800 (case)
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 Sensitive Lactose Sensitivity 22oz. plastic jar. 6 jars per case. Item numbers: 6499813 Retail UPCs: 055325001218

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-0926-2022
Lot/product code:
Batches: 26756SH00 34809SH00
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 17, 2022

Abbott Similac Pro-Sensitive Infant Formula with Iron 20.1oz. and 22.5oz. plastic jar. 4 jars per case; 34oz. plastic jar. 6 jars per case; 7oz. can. 6 cans per case. Item numbers: 66084 66657 67923 68090 Retail UPCs: 070074660820 070074666587 070074679242 070074680910

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-0930-2022
Lot/product code:
Batches: 23421SH00 24509SH00 24510SH00 24567SH00 24568SH00 25589SH00 25590SH00 25689SH00 26740SH00 26742SH00 26744SH00 24452SH00 24453SH00 24507SH00 24508SH00 25573SH00 25574SH00 25576SH00 25648SH00 25649SH00 26746SH00 26790SH00 26822SH00 26823SH00 27876SH00 27877SH00 29201SH00 29202SH00 29203SH00 29204SH01 29218SH00 29218SH01 29233SH00 29298SH00 29299SH00 30336SH00 31455SH00 31456SH00 31499SH00 31500SH00 32636SH00 32638SH00 33731SH00 33732SH00 33734SH00 34802SH00 34804SH00 35037SH00 35038SH00 35047SH00 35048SH00 35979SH00 35980SH00 35992SH00 35993SH00 36186SH00 36187SH00 36188SH00 36199SH00 36200SH00 25575K800 27953K800 27955K800 28023K800 28175K800 28176K800 29241K800 30320K800 30321K800 30337K800 31458K800 31589K800 33716K800 33733K800 27979SH00 27980SH00 27981SH00 28102SH00 28102SH10 28154SH00 28155SH00 28155SH01 28177SH00 29231SH00 29232SH00 30443SH00 30445SH00 31453SH00 32639SH00 35009SH00 35010SH00 35053SH00 35054SH00 35078SH00 35079SH00 35080SH00 36216SH00
Recalling firm:
Abbott Laboratories
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled February 17, 2022

Abbott Similac for Supplementation 22oz. plastic jar. 4 jars per case. Item numbers: 63013 Retail UPCs: 070074629506 70074629506

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-0922-2022
Lot/product code:
Batches: 24511SH00 27083SH00
Recalling firm:
Abbott Laboratories
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
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

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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
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

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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
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.

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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 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

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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 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

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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 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.

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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 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

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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)