FoodOct 5, 2022
Lamb Weston Sales Item GV020, Great Value Shredded Hash Browns, 4 lbs recall — FDA F-1806-2022
Potential to be contaminated with Listeria monocytogenes.
Class IIFDA: TerminatedLamb Weston Sales
Latest records
Latest recalls — page 674
The newest recall records with useful source details are listed here.
FoodOct 5, 2022
Belfonte Ice Cream & Dairy Foods Co 1.5 quarts recall — FDA F-1791-2022
The product may contain undeclared peanuts.
Class IFDA: TerminatedBelfonte Ice Cream & Dairy Foods Co
FoodOct 5, 2022
Hy-Vee, Inc. dba Hy-Vee Fresh Commissary HyVee Oven Baked Beans in 16 OZ plastic containers recall — FDA F-1808-2022
Baked bean product contains excessive amount of potassium sorbate
Class IIIFDA: TerminatedHy-Vee, Inc. dba Hy-Vee Fresh Commissary
FoodOct 5, 2022
Alida's Bakery 5 pieces per package recall — FDA F-1789-2022
Undeclared soy lecithin. The canola oil used to grease pans was found to contain soy lecithin.
Class IIIFDA: TerminatedAlida's Bakery LLC
FoodOct 5, 2022
Lamb Weston Sales Item SP204, Sprouts Organic Hash Browns Shredded Potatoes, 16 recall — FDA F-1807-2022
Potential to be contaminated with Listeria monocytogenes.
Class IIFDA: TerminatedLamb Weston Sales
FoodOct 5, 2022
Alida's Bakery 4 pieces per package, net wt recall — FDA F-1790-2022
Undeclared soy lecithin. The canola oil used to grease pans was found to contain soy lecithin.
Class IIIFDA: TerminatedAlida's Bakery LLC
DrugOct 5, 2022
Akorn Rifampin Capsules, USP, 300 mg, a) 30-count bottle (NDC 61748-018-30), b) 60-count recall — FDA D-1548-2022
Failed impurities/degradation specifications: Finished product exceeds the 5 ppm interim limit for 1-Methyl-4-Nitrosopoperazine (MNP).
Class IIFDA: OngoingAkorn, Inc.
DrugOct 5, 2022
Budesonide Inhalation Suspension 0.25mg/2mL, For Inhalation Only recall — FDA D-1545-2022
Lack of Assurance of Sterility
Class IIFDA: TerminatedCIPLA
DrugOct 5, 2022
Neoral soft gelatin capsules recall — FDA D-1543-2022
CGMP deviations: Out of specification results obtained during routine stability testing for ethanol content.
Class IIFDA: TerminatedNovartis Pharmaceuticals Corporation
DrugOct 5, 2022
Esomeprazole Magnesium Delayed-Release Capsules, USP, 40mg recall — FDA D-0005-2023
Superpotent Drug: Out of specification for assay at the 12-month timepoint.
Class IIIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugOct 5, 2022
QuVa Pharma oxyTOCIN 30 Units/500 mL (0.06 Units/mL) added to 0.9% Sodium Chloride recall — FDA D-1544-2022
Incorrect Product Formulation: Oxytocin 30 units was added to an IV bag of 0.45% Sodium Chloride (500mL) instead of 0.9% Sodium Chloride (500mL).
Class IIIFDA: TerminatedQuVa Pharma, Inc.
DrugOct 5, 2022
Viatris Ampicillin for Injection, USP, 2 grams/vial NDC 67457-352-02 recall — FDA D-1542-2022
Presence of Particulate Matter: A complaint was received for the presence of a single strand of hair in one vial.
Class IIFDA: TerminatedViatris Inc.
DrugOct 5, 2022
Esomeprazole Magnesium Delayed-Release Capsules, USP 20mg recall — FDA D-0004-2023
Superpotent Drug: Out of specification for assay at the 12-month timepoint.
Class IIIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
VehicleOct 5, 2022
Volkswagen Group of display function recall — NHTSA campaign 22V742000
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2021 Audi A8, RS7, RS6 Avant, RS5 Sportback, RS5 Coupe, Q8, Q7, Q5 Sportback, S4 Sedan, Q5, A7, A6, A6 Allroad, A5…
display functionVolkswagen Group of America, Inc.
VehicleSep 30, 2022
Maverick brake lights recall — NHTSA campaign 22V730000
Ford Motor Company (Ford) is recalling certain 2022 Maverick vehicles. Under certain circumstances, the Antilock Brake System (ABS) module may cause the brake lights to illuminate without…
brake lightsFord Motor Company
VehicleSep 29, 2022
General Motors seats recall — NHTSA campaign 22V724000
General Motors, LLC (GM) is recalling certain 2022-2023 Chevrolet Equinox and 2022 GMC Terrain vehicles. The driver's seat may have a stripped or loose bolt at the seat frame height-adjust…
seatsGeneral Motors, LLC
Medical DeviceSep 28, 2022
Paragon 28 Grappler Suture Anchor, Titanium, 3.0 x 10mm, Sterile Kit, REF: P44-110-3010-SK recall — FDA Z-1776-2022
Suture anchor may break upon insertion, which could lead to potential debris in patient, and delays in surgery.
Class IIFDA: OngoingParagon 28, Inc.
Medical DeviceSep 28, 2022
CAREFUSION BD MaxGuard Extension Set, REF: ME1069 recall — FDA Z-1753-2022
Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may…
Class IIFDA: OngoingCAREFUSION
Medical DeviceSep 28, 2022
CAREFUSION BD MaxGuard Extension Set with 4-way stopcock, REF: M4058 recall — FDA Z-1752-2022
Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may…
Class IIFDA: OngoingCAREFUSION
Medical DeviceSep 28, 2022
CAREFUSION BD MaxGuard Extension Set with 2 Needleless Y-Site, REF: MX9059 recall — FDA Z-1757-2022
Administration set, and extension set product labels list expiration year 2027 but the labels should list expiration year 2025. If expired product is used, the integrity of the product may…
Class IIFDA: OngoingCAREFUSION
Medical DeviceSep 28, 2022
Maquet Medical Systems USA BEQ-HLS 5050 USA; HLS Set Advanced 5.0 Part No. 70106.9077. A recall — FDA Z-1766-2022
The firm has expanded the recall for the HLS Set Advanced regarding a potential breach in the sterility barrier that may result in compromised product sterility (prior recall was initiated…
Class IIFDA: OngoingMaquet Medical Systems USA
Medical DeviceSep 28, 2022
Maquet Medical Systems USA BEQ-HLS 7050 USA; HLS Set Advanced 7.0 Part No. 70106.9078. A recall — FDA Z-1767-2022
The firm has expanded the recall for the HLS Set Advanced regarding a potential breach in the sterility barrier that may result in compromised product sterility (prior recall was initiated…
Class IIFDA: OngoingMaquet Medical Systems USA
Medical DeviceSep 28, 2022
Maquet Medical Systems USA BEQ-HLS 7050 USA; HLS Set Advanced 7.0 Part No. 70105.2794. A recall — FDA Z-1764-2022
The firm has expanded the recall for the HLS Set Advanced regarding a potential breach in the sterility barrier that may result in compromised product sterility (prior recall was initiated…
Class IIFDA: OngoingMaquet Medical Systems USA
Medical DeviceSep 28, 2022
Fresenius Medical Care Holdings AquaC UNO H [120V, 60Hz, 1700VA, US-Version- a reverse recall — FDA Z-1770-2022
Internal ethemet cables are missing one or both ferrite cores therefore the electromagnetic compatibility of the device is not ensured
Class IIFDA: OngoingFresenius Medical Care Holdings, Inc.
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Recent recall archives
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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