FoodJun 16, 2021
BCFoods BC Foods AD Celery Stalk Canners, 25 lb recall — FDA F-0673-2021
Product contains ingredient which tested positive for Salmonella
Class IFDA: TerminatedBCFoods, Inc.
Monthly breakdown
2021 recalls by month
Select a month to review the recall records reported during that period.
December 2021194 records · 4 categoriesNovember 2021210 records · 4 categoriesOctober 2021342 records · 4 categoriesSeptember 2021300 records · 4 categoriesAugust 2021279 records · 4 categoriesJuly 2021251 records · 4 categoriesJune 2021361 records · 4 categoriesMay 2021226 records · 4 categoriesApril 2021279 records · 4 categoriesMarch 2021241 records · 4 categoriesFebruary 2021320 records · 4 categoriesJanuary 2021226 records · 4 categories
2021 recalls — page 76
Records are ordered by the best available source date.
FoodJun 16, 2021
Gilster-Mary Lee Organic Microwave Butter Popcorn in cartons labeled to be recall — FDA F-0659-2021
Butter microwave popcorn bags were packaged in organic salted popcorn consumer boxes and therefore contain undeclared milk
Class IFDA: TerminatedGilster-Mary Lee Corp.
FoodJun 16, 2021
BCFoods BC Foods Celery Stalk and Leaf Dice 3/8, AD Sulfites, 11 lb recall — FDA F-0674-2021
Product contains ingredient which tested positive for Salmonella
Class IFDA: TerminatedBCFoods, Inc.
FoodJun 16, 2021
The Kroger Co Chicken Street Taco kit in a plastic tray with a clear plastic recall — FDA F-0678-2021
Undeclared egg allergen for Chipotle Crema on product label.
Class IFDA: TerminatedThe Kroger Co
FoodJun 16, 2021
Sun Hong Foods Seafood Mushroom Keep Refrigerated Net Wt recall — FDA F-0750-2021
Potential L. mono contamination due to CDPH product sample findings.
Class IFDA: TerminatedSun Hong Foods, Inc.
FoodJun 16, 2021
The Coca-Cola Company Glaceau Vitaminwater XXX labeled to be Glaceau Vitaminwater recall — FDA F-0662-2021
Product labeled to be "zero sugar" may contain sugar due to an incorrect label being used.
Class IIFDA: TerminatedThe Coca-Cola Company
DrugJun 16, 2021
Fresenius Medical Care Holdings DELFLEX Peritoneal Dialysis Solution with 1.5% Dextrose, Low recall — FDA D-0607-2021
Temperature Abuse: Product exposed to temperature outside specified limits.
Class IIIFDA: TerminatedFresenius Medical Care Holdings, Inc.
DrugJun 16, 2021
Fresenius Medical Care Holdings DELFLEX Peritoneal Dialysis Solution with 1.5% Dextrose, Low recall — FDA D-0610-2021
Temperature Abuse: Product exposed to temperature outside specified limits.
Class IIIFDA: TerminatedFresenius Medical Care Holdings, Inc.
DrugJun 16, 2021
Fresenius Medical Care Holdings DELFLEX Peritoneal Dialysis Solution with 2.5% Dextrose, Low recall — FDA D-0608-2021
Temperature Abuse: Product exposed to temperature outside specified limits.
Class IIIFDA: TerminatedFresenius Medical Care Holdings, Inc.
DrugJun 16, 2021
READYPREP CHG, 2% Chlorhexidine Gluconate Cloth, 2 9x10.5 in (22.9x26.7 cm) Disposable recall — FDA D-0624-2021
Superpotent Drug: Product is above specification for active ingredient, 2% Chlorhexidine Gluconate.
Class IIIFDA: TerminatedMedline Industries Inc.
DrugJun 16, 2021
McKesson Corporation dba McKesson Drug Company Levetiracetam Tablets USP, 250 mg UD 100 recall — FDA D-0630-2021
Labeling; Wrong Barcode; error in the machine-readable barcode which could result in some units being read as Naproxen Tablets 500 mg. Product is labeled correctly as Levetiracetam
Class IIIFDA: TerminatedMcKesson Corporation dba McKesson Drug Company
DrugJun 16, 2021
Fresenius Medical Care Holdings DELFLEX Peritoneal Dialysis Solution with 2.5 % Dextrose recall — FDA D-0605-2021
Temperature Abuse: Product exposed to temperature outside specified limits.
Class IIIFDA: TerminatedFresenius Medical Care Holdings, Inc.
DrugJun 16, 2021
Fresenius Medical Care Holdings DELFLEX Peritoneal Dialysis Solution with 4.25% Dextrose recall — FDA D-0609-2021
Temperature Abuse: Product exposed to temperature outside specified limits.
Class IIIFDA: TerminatedFresenius Medical Care Holdings, Inc.
VehicleJun 10, 2021
General Motors stand recall — NHTSA campaign 21V440000
General Motors, LLC. (GM) is recalling certain 2020-2022 Buick Encore GX and 2021-2022 Chevrolet Trailblazer vehicles. The emergency jack, if not positioned as directed in the vehicle…
standGeneral Motors, LLC
VehicleJun 10, 2021
General Motors srs malfunction warning lamp/light recall — NHTSA campaign 21V421000
General Motors, LLC (GM) is recalling certain 2021 Buick Envision, Cadillac CT4, CT5, Escalade, Escalade ESV, Chevrolet Tahoe, Corvette, Suburban, GMC Yukon, Yukon XL vehicles. The…
srs malfunction warning lamp/lightGeneral Motors, LLC
VehicleJun 10, 2021
Ram 1500 display function recall — NHTSA campaign 21V438000
Chrysler (FCA US, LLC) is recalling certain 2021 Ram 1500 vehicles equipped with a trailer reverse steering module (TRSCM). The rearview camera image may not display. As such, these…
display functionChrysler (FCA US, LLC)
VehicleJun 10, 2021
Chrysler oil/lubrication recall — NHTSA campaign 21V439000
Chrysler (FCA US, LLC) is recalling certain 2019-2020 Ram 3500, 4500, and 5500 cab chassis vehicles equipped with a Cummins 6.7L High Output engine. The engine calibration software may not…
oil/lubricationChrysler (FCA US, LLC)
Medical DeviceJun 9, 2021
Terumo Cardiovascular Systems The Terumo HX2 Temperature Management System provides recall — FDA Z-1789-2021
Terumo CVS has been unable to validate a cleaning protocol to satisfy current regulatory concerns and expectations. As a result, an updated cleaning protocol will not be developed by Terumo…
Class IIFDA: TerminatedTerumo Cardiovascular Systems Corporation
Medical DeviceJun 9, 2021
Zavation InterV, 10G Kyphoplasty Kits, REF numbers: a) INTVM-10-DSK b) INTVM-10-SBK c) recall — FDA Z-1751-2021
Products distributed as sterile may not have been adequately sterilized
Class IIFDA: TerminatedZavation
Medical DeviceJun 9, 2021
Medtronic Minimed MiniMed 780G Insulin Pump: Models: PUMP MMT-1885 MM780G 6.5V BLE MMOL;¿ recall — FDA Z-1771-2021
Due to a software design issue, under certain conditions, a software fault is detected when a large bolus delivery at quick bolus speed completes. if the user is not aware of the amount of…
Class IIFDA: OngoingMedtronic Minimed
Medical DeviceJun 9, 2021
K2M Cascadia AN Interbody Convex 10x22x14mm recall — FDA Z-1695-2021
Mislabeled product labeling references incorrect length or height, or length and height for specific Lots, Sizes 10x22x14mm, 10x28x14mm, 10x22x15mm
Class IIFDA: TerminatedK2M, Inc.
Medical DeviceJun 9, 2021
Fujifilm Medical Systems U.S.A Synapse Cardiovascular (Synapse CV) recall — FDA Z-1775-2021
Software versions 6.0.4 to 6.2.1 using Advanced Reporting -possibility that a previously assigned internal patient database ID can be reused for a new patient. It was discovered that this…
Class IIFDA: TerminatedFujifilm Medical Systems U.S.A., Inc.
Medical DeviceJun 9, 2021
Siemens Medical Solutions USA Multitom RAX with software version VF10 recall — FDA Z-1685-2021
Siemens identified two issues, In some cases, it is possible to perform an image acquisition although more than 20% of the beam does not hit the detector. This may only occur when an organ…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Medical DeviceJun 9, 2021
LEPU MEDICAL TECHNOLOGY (BEIJING) CO Leccurate SARS-CoV-2, Antigen Rapid Test Kit recall — FDA Z-1620-2021
Antigen Rapid Test Kit is not authorized, cleared, or approved for marketing and/or distribution in the U.S.
Class IFDA: CompletedLEPU MEDICAL TECHNOLOGY (BEIJING) CO., LTD
About the 2021 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.