FoodFeb 3, 2021
Samyang Buldak Carbonara Hot Chicken Flavor Sauce Hot Chili recall — FDA F-0238-2021
Undeclared wheat, egg, and coconut oil
Class IIFDA: TerminatedSamyang Foods Co Ltd
Latest records
Latest recalls — page 912
The newest recall records with useful source details are listed here.
FoodFeb 3, 2021
Port City Bakery Dough Shop Par Baked Crust, frozen pizza crusts packaged in recall — FDA F-0225-2021
Frozen pizza crust may contain foreign material (glass).
Class IIFDA: TerminatedPort City Bakery, Inc.
FoodFeb 3, 2021
Weis Quality Cookies and Cream Ice Cream recall — FDA F-0218-2021
Ice Cream product may contain metal (foreign objects).
Class IIFDA: TerminatedWeis Markets, Inc., Ice Cream Division
FoodFeb 3, 2021
Samyang Buldak Extremely Spicy Hot Chicken Flavor Sauce Hot recall — FDA F-0237-2021
Undeclared allergens of egg, milk, and wheat
Class IIFDA: TerminatedSamyang Foods Co Ltd
FoodFeb 3, 2021
Port City Bakery AK 10 5/8" Par Baked Stuffed Crust, frozen Pizza Crust, Item recall — FDA F-0222-2021
Frozen pizza crust may contain foreign material (glass).
Class IIFDA: TerminatedPort City Bakery, Inc.
FoodFeb 3, 2021
Nueske Applewood Smoked Meat Cinnamon Walnut Coffee Cake, Item 258, Net Wt recall — FDA F-0241-2021
Coffee cake may contain undeclared wheat, egg, milk, and walnuts.
Class IIFDA: TerminatedNueske Applewood Smoked Meat, Inc.
DrugFeb 3, 2021
Ketorolac Tromethamine Injection, USP, 30 mg per mL recall — FDA D-0245-2021
Presence of Particulate Matter - found in reserve sample vials at the firm.
Class IFDA: TerminatedFresenius Kabi USA, LLC
DrugFeb 3, 2021
Shane Erickson IMC Wash-Free Hand Sanitizer, (ethyl alcohol), 75%, 10.1 fl. oz. (300 ml) recall — FDA D-0241-2021
CGMP Deviations: product manufactured at the same facility that produced product that FDA sampled and found to be subpotent for ethanol and contained methanol.
Class IIFDA: TerminatedShane Erickson Inc.
DrugFeb 3, 2021
Shane Erickson IMC Wash-Free Hand Sanitizer, (ethyl alcohol), 75%, 3.4 fl. oz. (100 ml) recall — FDA D-0240-2021
CGMP Deviations: product manufactured at the same facility that produced product that FDA sampled and found to be subpotent for ethanol and contained methanol.
Class IIFDA: TerminatedShane Erickson Inc.
DrugFeb 3, 2021
Shane Erickson IMC Wash-Free Hand Sanitizer, (ethyl alcohol), 75%, 1.7 fl. oz. (50 ml) recall — FDA D-0239-2021
CGMP Deviations: product manufactured at the same facility that produced product that FDA sampled and found to be subpotent for ethanol and contained methanol.
Class IIFDA: TerminatedShane Erickson Inc.
DrugFeb 3, 2021
Bausch Health Companies Phytonadione Tablets 5mg, 30-count bottle recall — FDA D-0244-2021
Failed Impurities/Degradation Specifications:Out of specification during the 24 month stability testing of Impurity D.
Class IIIFDA: TerminatedBausch Health Companies, Inc.
VehicleFeb 1, 2021
Volkswagen Group of seats recall — NHTSA campaign 21V038000
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2021 Volkswagen Tiguan Long Wheelbase and Jetta vehicles. Bolts may be missing from the front seat tracks.
seatsVolkswagen Group of America, Inc.
VehicleFeb 1, 2021
Ram 1500 Classic SLT trucks. Certain master cylinder recall — NHTSA campaign 21V037000
Chrysler (FCA US, LLC) is recalling certain 2020-2021 Ram 1500 Classic SLT trucks. Certain vehicles were built without the retaining clip that secures the master cylinder push rod to the…
master cylinderChrysler (FCA US, LLC)
VehicleJan 29, 2021
BMW column recall — NHTSA campaign 21V031000
BMW of North America, LLC (BMW) is recalling certain 2021 X5 sDrive40i, X5 xDrive40i, X5M, X5 xDrive45e, X6 sDrive40i, X6 xDrive40i, X7 xDrive40i, X7 M50i vehicles. The steering column…
columnBMW of North America, LLC
VehicleJan 28, 2021
Chrysler clutch recall — NHTSA campaign 21V028000
Chrysler (FCA US, LLC) is recalling certain 2018-2021 Jeep Wrangler and 2020-2021 Jeep Gladiator vehicles equipped with manual transmissions. The clutch pressure plate may overheat and…
clutchChrysler (FCA US, LLC)
Medical DeviceJan 27, 2021
Fujifilm Medical Systems U.S.A Synapse PACS Software Versions 5.1 and higher recall — FDA Z-0878-2021
There is a potential for the wrong patient information may be displayed in the viewer or PowerJacket. Additionally, the incorrect max standard uptake values (SUV) for PET ad CT studies may…
Class IIFDA: OngoingFujifilm Medical Systems U.S.A., Inc.
Medical DeviceJan 27, 2021
Penumbra JET 7 KIT Reperfusion Catheter+Penumbra Hi-Flow Aspiration Tubing REF recall — FDA Z-0850-2021
The catheter may become susceptible to distal tip damage during use. Distal tip damage in conjunction with pressurization of contrast injection may result in potential vessel damage, and…
Class IFDA: TerminatedPenumbra Inc.
Medical DeviceJan 27, 2021
Boston Scientific ACUITY Universal Cutter, MODEL 7060 - Product Usage: intended to recall — FDA Z-0870-2021
Boston Scientific (BSC) is retrieving five Model 7060 ACUITY cutters distributed in the US that did not undergo the applicable sterile processing procedure.
Class IIFDA: TerminatedBoston Scientific Corporation
Medical DeviceJan 27, 2021
Skeletal Kinetics OsteoVation, Inject, Bone Filler Kits 10cc recall — FDA Z-0867-2021
A discrepancy was found between the Mixing Instruction Card and the Instructions for Use for the 5cc and 10 cc bone void filler kits. No customer complaints or reports of injury have been…
Class IIFDA: TerminatedSkeletal Kinetics, LLC
Medical DeviceJan 27, 2021
Beckman Coulter ACCESS SARS-CoV-2 IgG QC SARS-CoV-2 IgG REF C58964 - Product Usage: use on recall — FDA Z-0875-2021
The Quality Control (QC) card has a label error for the standard deviation (SD) values for one out of the two levels of QC.
Class IIFDA: TerminatedBeckman Coulter Inc.
Medical DeviceJan 27, 2021
Penumbra JET 7MAX KIT Penumbra JET 7 Reperfusion Catheter+ MAX Delivery Device + Hi-Flow recall — FDA Z-0851-2021
The catheter may become susceptible to distal tip damage during use. Distal tip damage in conjunction with pressurization of contrast injection may result in potential vessel damage, and…
Class IFDA: TerminatedPenumbra Inc.
Medical DeviceJan 27, 2021
Medtronic Neurosurgery REF 27219-1 X1, Medtronic, Delta Valve, Neonatal, Performance Level recall — FDA Z-0871-2021
Neonatal Valves were manufactured with a ventricular catheter connection site shorter than the design specification. The defect can lead to difficulty in securing the valve to the proximal…
Class IIFDA: OngoingMedtronic Neurosurgery
Medical DeviceJan 27, 2021
Smiths Medical ASD Portex Acapella DH Vibratory PEP Device - Product Usage: a single patient recall — FDA Z-0874-2021
Shipping box may contain wrong model.
Class IIFDA: TerminatedSmiths Medical ASD Inc.
Medical DeviceJan 27, 2021
Roche Diagnostics Operations A calculator/data processing module for clinical use is an recall — FDA Z-0883-2021
A software error results in the unintentional removal of the serum-indices flag that would otherwise prevent the release of results. The Cobas Inifinity has an auto-verification feature to…
Class IIFDA: TerminatedRoche Diagnostics Operations, Inc.
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
October 2026111 records · 4 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