FoodNov 10, 2021
POTANDON PRODUCE Green Giant Fresh whole RED onions in 2 lbs recall — FDA F-0116-2022
Potential to be contaminated with Salmonella Oranienburg.
Class IFDA: TerminatedPOTANDON PRODUCE LLC
Latest records
Latest recalls — page 802
The newest recall records with useful source details are listed here.
FoodNov 10, 2021
Kansas City LLC., DBA Best Harvest Bakeries Hamburger buns, 4.5" in unlabeled clear plastic recall — FDA F-0081-2022
Positive environmental samples analyzed for Listeria and Salmonella species.
Class IIFDA: TerminatedKansas City LLC., DBA Best Harvest Bakeries
FoodNov 10, 2021
Kansas City LLC., DBA Best Harvest Bakeries Hotdog buns, in unlabeled clear plastic bags, 30 recall — FDA F-0084-2022
Positive environmental samples analyzed for Listeria and Salmonella species.
Class IIFDA: TerminatedKansas City LLC., DBA Best Harvest Bakeries
DrugNov 10, 2021
Lupin Pharmaceuticals Irbesartan and Hydrochlorothiazide Tablets USP, 150/12.5 mg a) 30 recall — FDA D-0089-2022
CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Class IIFDA: TerminatedLupin Pharmaceuticals Inc.
DrugNov 10, 2021
Bryant Ranch Prepack, Inc. dba BRP Methocarbamol 500mg Tablet recall — FDA D-0092-2022
Labeling: Label Error on Declared Strength; Bottles labeled as Methocarbamol 500 mg Tablets actually contain Methocarbamol 750 mg Tablets
Class IFDA: CompletedBryant Ranch Prepack, Inc. dba BRP Pharmaceuticals
DrugNov 10, 2021
MERCK SHARP & DOHME Cubicin (daptomycin for injection), 500 mg per vial, Single-dose vial recall — FDA D-0093-2022
Presence of Particulate Matter: Identified as Glass Particles
Class IFDA: TerminatedMERCK SHARP & DOHME CORP
DrugNov 10, 2021
EZETIMIBE AND SIMVASTATIN Dr. Reddy's Ezetimibe and Simvastatin Tablets, 10 mg/10 mg, a) 90 recall — FDA D-0081-2022
Failed Excipient Specifications; product manufactured using an excipient found to be OOS for conductivity
Class IIFDA: TerminatedDr. Reddy's Laboratories, Inc.
DrugNov 10, 2021
EZETIMIBE AND SIMVASTATIN Dr. Reddy's Ezetimibe and Simvastatin Tablets, 10 mg/40 mg, 500 recall — FDA D-0085-2022
Failed Excipient Specifications and Presence of Foreign Tablets/Capsules; product manufactured using an excipient found to be OOS for conductivity and some Ezetimibe and Simvastatin…
Class IIFDA: TerminatedDr. Reddy's Laboratories, Inc.
DrugNov 10, 2021
EZETIMIBE AND SIMVASTATIN Dr. Reddy's Ezetimibe and Simvastatin Tablets, 10 mg/80 mg, a) 30 recall — FDA D-0083-2022
Failed Excipient Specifications; product manufactured using an excipient found to be OOS for conductivity
Class IIFDA: TerminatedDr. Reddy's Laboratories, Inc.
DrugNov 10, 2021
EZETIMIBE AND SIMVASTATIN Dr. Reddy's Ezetimibe and Simvastatin Tablets, 10 mg/20 mg, a) 30 recall — FDA D-0082-2022
Failed Excipient Specifications; product manufactured using an excipient found to be OOS for conductivity
Class IIFDA: TerminatedDr. Reddy's Laboratories, Inc.
DrugNov 10, 2021
EZETIMIBE AND SIMVASTATIN Dr. Reddy's Ezetimibe and Simvastatin Tablets, 10 mg/40 mg, a) 30 recall — FDA D-0084-2022
Failed Excipient Specifications; product manufactured using an excipient found to be OOS for conductivity
Class IIFDA: TerminatedDr. Reddy's Laboratories, Inc.
DrugNov 10, 2021
Lupin Pharmaceuticals Irbesartan and Hydrochlorothiazide Tablets USP, 300/12.5 mg a) 30 recall — FDA D-0090-2022
CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Class IIFDA: TerminatedLupin Pharmaceuticals Inc.
VehicleNov 10, 2021
Volkswagen Group of seats recall — NHTSA campaign 21V874000
Volkswagen Group of America, Inc. (Audi) is recalling certain 2017-2020 A4 Allroad, A4 Sedan, 2018-2019 RS5 Coupe, 2019 RS5 Sportback, 2018-2020 A5 Cabriolet, A5 Coupe, A5 Sportback, S4…
seatsVolkswagen Group of America, Inc.
VehicleNov 10, 2021
Ford traction battery recall — NHTSA campaign 21V869000
Ford Motor Company (Ford) is recalling one 2021 Escape vehicle equipped with a 2.5L hybrid powertrain. The high voltage battery may fail, resulting in a sudden loss of drive power.
traction batteryFord Motor Company
VehicleNov 10, 2021
Ford rear recall — NHTSA campaign 21V870000
Ford Motor Company (Ford) is recalling certain 2021 Explorer and Lincoln Aviator vehicles. Incorrect rear suspension module components may have been installed due to a labeling error.
rearFord Motor Company
VehicleNov 10, 2021
Chrysler air bag control module software recall — NHTSA campaign 21V873000
Chrysler (FCA US, LLC) is recalling certain 2021 Jeep Grand Cherokee L, 2022 Jeep Wagoneer, and Grand Wagoneer vehicles. The Occupant Restraint Controller (ORC) may have incorrect software…
air bag control module softwareChrysler (FCA US, LLC)
VehicleNov 10, 2021
Ram 1500 electrical heating element recall — NHTSA campaign 21V871000
Chrysler (FCA US, LLC) is recalling certain 2022 Ram 1500 vehicles. These vehicles may have been built with incompatible heating, ventilation, and air conditioning systems (HVAC), resulting…
electrical heating elementChrysler (FCA US, LLC)
VehicleNov 9, 2021
Tesla air bags recall — NHTSA campaign 21V868000
Tesla, Inc. (Tesla) is recalling certain 2021 Model X and Model S vehicles. The driver's air bag cushion may tear during deployment.
air bagsTesla, Inc.
Medical DeviceNov 3, 2021
W L Gore & Associates REF/Catalogue Number GSXE0025, GORE CARDIOFORM SEPTAL OCCLUDER 25 mm recall — FDA Z-0168-2022
Septal Occluders contain the incorrect expiration date. Product is labeled with a 3 yr. expiration date instead of 2 yrs.
Class IIFDA: OngoingW L Gore & Associates, Inc.
Medical DeviceNov 3, 2021
W L Gore & Associates REF/Catalogue Number GSX0030A, GORE CARDIOFORM SEPTAL OCCLUDER 30 mm recall — FDA Z-0164-2022
Septal Occluders contain the incorrect expiration date. Product is labeled with a 3 yr. expiration date instead of 2 yrs.
Class IIFDA: OngoingW L Gore & Associates, Inc.
Medical DeviceNov 3, 2021
W L Gore & Associates REF/Catalogue Number GSXE0020, GORE CARDIOFORM SEPTAL OCCLUDER 20 mm recall — FDA Z-0167-2022
Septal Occluders contain the incorrect expiration date. Product is labeled with a 3 yr. expiration date instead of 2 yrs.
Class IIFDA: OngoingW L Gore & Associates, Inc.
Medical DeviceNov 3, 2021
Xstrahl Concerto User Interface Software provided with the following systems: (1) Xstrahl recall — FDA Z-0174-2022
If a saved treatment plan with 2 opposing beams is edited prior to approval, then Beam 2 is not updated with the changed parameters upon selecting save, resulting in error messages during…
Class IIFDA: TerminatedXstrahl Limited
Medical DeviceNov 3, 2021
Smiths Medical ASD Bivona Uncuffed Wire Endotracheal Tubes recall — FDA Z-0178-2022
Inadequate pouch seal leading to a compromised sterile barrier on products with a shaft length of 325mm.
Class IIFDA: TerminatedSmiths Medical ASD Inc.
Medical DeviceNov 3, 2021
Siemens Healthcare Diagnostics Atellica CH Urinary/Cerebrospinal Fluid Protein (UCFP), SMN recall — FDA Z-0180-2022
The firm has confirmed the potential for Atellica CH Urinary/Cerebrospinal Fluid Protein reagent carryover impacting Enzymatic Hemoglobin A1c (A1c_E and A1c_EM) results. Falsely depressed…
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
Browse by month
Recent recall archives
Browse recent months with enough recall history for useful comparison.
October 2026110 records · 3 categoriesSeptember 2026364 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categories