FoodJan 20, 2021
Ocean Providence Minneapolis Frozen Ground Tuna, Wild Caught, Production Date: 06/01/2020 recall — FDA F-0204-2021
Ground Tuna may contain elevated levels of Histamine.
Class IIFDA: TerminatedOcean Providence Minneapolis LLC
Latest records
Latest recalls — page 917
The newest recall records with useful source details are listed here.
DrugJan 20, 2021
KVK-Tech Benzhydrocodone and Acetaminophen Tablets, CII, 6.12mg/ 325mg, 100 Tablets recall — FDA D-0224-2021
Failed Impurities/Degradation Specifications; out of specification results obtained for N-Oxide impurity during the 12-month long term stability testing for Batch# 15892A
Class IIIFDA: TerminatedKVK-Tech, Inc.
DrugJan 20, 2021
GAZA PROVEEDORA DE SERVICIOS DE HOSPEDAJE Y Pristine gel Hand Sanitizer Gel Antibacterial recall — FDA D-0229-2021
cGMP deviations: Product made at the same facility where product tested was sub-potent.
Class IIFDA: OngoingGAZA PROVEEDORA DE SERVICIOS DE HOSPEDAJE Y…
DrugJan 20, 2021
GAZA PROVEEDORA DE SERVICIOS DE HOSPEDAJE Y Zapien Productos Hand Sanitizer Gel recall — FDA D-0230-2021
cGMP deviations: Product made at the same facility where product tested was sub-potent.
Class IIFDA: OngoingGAZA PROVEEDORA DE SERVICIOS DE HOSPEDAJE Y…
DrugJan 20, 2021
Oxycodone Hydrochloride Oral Solution, USP 5 mg/5mL unit dose cups recall — FDA D-0231-2021
Presence of Foreign Substance: Particulate matter was found in multiple lots of product.
Class IIIFDA: TerminatedGenus Lifesciences Inc.
DrugJan 20, 2021
Edge Pharma Methotrexate, USP Sterile Solution for Injection, Preservative Free 125mg/5ml recall — FDA D-0226-2021
Lack of Assurance of Sterility; the media used to conduct post-compounding sterility testing for the Methotrexate product was expired.
Class IIFDA: TerminatedEdge Pharma, LLC
DrugJan 20, 2021
US Compounding Succinylcholine Chloride PF Inj. 200 mg/10 mL, 10 mL single use syringes recall — FDA D-0223-2021
Labeling: Incorrect or Missing lot and/or expiration date: The lot number and BUD were printed in the incorrect position on the product label making it illegible.
Class IIIFDA: TerminatedUS Compounding Inc.
DrugJan 20, 2021
Precision Dose Chlorhexidine Gluconate Oral Rinse USP 0.12% recall — FDA D-0228-2021
cGMP deviations: The firm was notified of the manufacturer's expanded recall.
Class IIFDA: TerminatedPrecision Dose Inc.
DrugJan 20, 2021
Sunstar Americas Paroex (Chlorhexidine Gluconate) Oral Rinse, USP 0.12%, Alcohol Free recall — FDA D-0222-2021
cGMP Deviations; FDA inspection of manufacturing facility observed potential Burkholderia cepacia complex (BCC) contamination, inadequate cleaning, inadequate microbiological testing, and…
Class IIFDA: OngoingSunstar Americas, Inc.
VehicleJan 15, 2021
Ford driveshaft recall — NHTSA campaign 21V011000
Ford Motor Company (Ford) is recalling certain 2020-2021 Edge, 2020 Lincoln Nautilus and Ford Escape and 2021 Lincoln Corsair and Ford Bronco Sport vehicles. An inadequate amount of…
driveshaftFord Motor Company
VehicleJan 14, 2021
Braun-modified Honda Odyssey storage recall — NHTSA campaign 21V010000
Braun Corporation (Braun) is recalling certain 2018-2021 Braun-modified Honda Odyssey vehicles. The fuel tank assembly installed by Braun may be susceptible to the fuel tank overfilling…
storageBraun Corporation
Medical DeviceJan 13, 2021
Steris Vis-U-All High Temperature Tubing 4"x100' recall — FDA Z-0787-2021
Purple ink located on the outside label of Vis-U-All Pouches may migrate (bleed) following steam processing causing cosmetic defects on the exterior of the pouch and in some instances,…
Class IIFDA: TerminatedSteris Corporation
Medical DeviceJan 13, 2021
Smith & Nephew Bone fixation nail recall — FDA Z-0772-2021
Manufacturing packaging error.
Class IIFDA: TerminatedSmith & Nephew, Inc.
Medical DeviceJan 13, 2021
Accuray TomoTherapy Treatment System - Product Usage: used as an integrated system for the recall — FDA Z-0784-2021
"MLC tickle error" may result in the delivered dose to effectively rotate from the planned dose.
Class IIFDA: TerminatedAccuray Inc.
Medical DeviceJan 13, 2021
Boston Scientific AXIOS Stent and Electrocautery - Enhanced Delivery System 10mm x15mm UPN recall — FDA Z-0774-2021
The rotating luer fitting at the distal end of the delivery system handle may become detached from the nose of the delivery during device preparation, stent delivery or use, resulting in…
Class IIFDA: TerminatedBoston Scientific Corporation
Medical DeviceJan 13, 2021
Steris Vis-U-All High Temperature Tubing 3"x100' recall — FDA Z-0786-2021
Purple ink located on the outside label of Vis-U-All Pouches may migrate ( bleed ) following steam processing causing cosmetic defects on the exterior of the pouch and in some instances,…
Class IIFDA: TerminatedSteris Corporation
Medical DeviceJan 13, 2021
Steris Vis-U-All High Temp 4.5"x11" Heat Seal Pouch 200 pouches per box recall — FDA Z-0790-2021
Purple ink located on the outside label of Vis-U-All Pouches may migrate ( bleed ) following steam processing causing cosmetic defects on the exterior of the pouch and in some instances,…
Class IIFDA: TerminatedSteris Corporation
Medical DeviceJan 13, 2021
Boston Scientific Hot AXIOS Stent and Electrocautery - Enhanced Delivery System 10mm x10mm recall — FDA Z-0776-2021
The rotating luer fitting at the distal end of the delivery system handle may become detached from the nose of the delivery during device preparation, stent delivery or use, resulting in…
Class IIFDA: TerminatedBoston Scientific Corporation
Medical DeviceJan 13, 2021
Steris Vis-U-All High Temp 7.5"x13" Self Seal Pouch 200 pouches per box recall — FDA Z-0798-2021
Purple ink located on the outside label of Vis-U-All Pouches may migrate ( bleed ) following steam processing causing cosmetic defects on the exterior of the pouch and in some instances,…
Class IIFDA: TerminatedSteris Corporation
Medical DeviceJan 13, 2021
Boston Scientific AXIOS Stent and Electrocautery - Enhanced Delivery System 10mm x10mm UPN recall — FDA Z-0773-2021
The rotating luer fitting at the distal end of the delivery system handle may become detached from the nose of the delivery during device preparation, stent delivery or use, resulting in…
Class IIFDA: TerminatedBoston Scientific Corporation
Medical DeviceJan 13, 2021
Steris Vis-U-All High Temp 8"x16" Self Seal Pouch 200 pouches per box recall — FDA Z-0799-2021
Purple ink located on the outside label of Vis-U-All Pouches may migrate ( bleed ) following steam processing causing cosmetic defects on the exterior of the pouch and in some instances,…
Class IIFDA: TerminatedSteris Corporation
Medical DeviceJan 13, 2021
Steris Vis-U-All High Temp 5"x15" Self Seal Pouch 200 pouches per box recall — FDA Z-0797-2021
Purple ink located on the outside label of Vis-U-All Pouches may migrate ( bleed ) following steam processing causing cosmetic defects on the exterior of the pouch and in some instances,…
Class IIFDA: TerminatedSteris Corporation
Medical DeviceJan 13, 2021
Steris Vis-U-All High Temp 4"x11" Self Seal Pouch 200 pouches per box recall — FDA Z-0795-2021
Purple ink located on the outside label of Vis-U-All Pouches may migrate ( bleed ) following steam processing causing cosmetic defects on the exterior of the pouch and in some instances,…
Class IIFDA: TerminatedSteris Corporation
Medical DeviceJan 13, 2021
Medline Industries Greffe Aorte-LF recall — FDA Z-0782-2021
The cylindrical sponge component is not x-ray detectable.
Class IIFDA: TerminatedMedline Industries 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