FoodSep 24, 2025
HI-TECH PHARMACEUTICALS BETA SITOSTEROL recall — FDA H-0588-2025
Unapproved Drug Claims and Misbranded.
Class IIIFDA: TerminatedHi-Tech Pharmaceuticals Inc.
Latest records
Latest recalls — page 173
The newest recall records with useful source details are listed here.
FoodSep 24, 2025
Admiralty Island Fisheries Inc dba AquaStar Frozen AquaStar Breaded Shrimp, Butterfly recall — FDA H-0585-2025
Product may be contaminated with Cesium-137 (Cs-137).
Class IIFDA: OngoingAdmiralty Island Fisheries Inc dba AquaStar (USA) Corp.
FoodSep 24, 2025
Wang Globalnet recall — FDA H-0611-2025
Oyster product potentially contaminated with Norovirus
Class IIFDA: TerminatedWang Globalnet
FoodSep 24, 2025
Hi-Tech Pharmaceuticals PRIMENUTRITION TAURINE MENTAL & ATHLETIC PERFORMANCE 125 recall — FDA H-0598-2025
Unapproved Drug Claims and Misbranded.
Class IIIFDA: TerminatedHi-Tech Pharmaceuticals Inc.
DrugSep 24, 2025
Sulfamethoxazole and Trimethoprim Tablets, USP 800mg / 160mg Double Strength recall — FDA D-0654-2025
Presence of a Foreign Substance: A specific lot of auxiliary polyester coil, used in product packaging by manufacturer (Amneal Pharmaceuticals LLC) was detected with presence of a…
Class IIFDA: OngoingNorthwind Pharmaceuticals LLC
DrugSep 24, 2025
Cyclophosphamide Injection 500 mg/5 mL (100 mg/mL), Hazardous Drug recall — FDA D-0651-2025
cGMP deviations: Temperature excursion during transportation.
Class IIFDA: OngoingSandoz Inc
DrugSep 24, 2025
Cyclobenzaprine Hydrochloride Tablets, USP, 10 mg, 90-count bottle recall — FDA D-0655-2025
Labeling: Label Mix Up; Bottles of Meloxicam USP, 7.5mg, 90-count tablets (yellow in color), were labeled as Cyclobenzaprine Hydrochloride Tablets USP, 10 mg 90-count tablets (blue in…
Class IFDA: OngoingUnichem Pharmaceuticals USA Inc.
DrugSep 24, 2025
chlorproMAZINE Hydrochloride Tablets, USP, 25 mg, packaged as a) 50 (5x10) blisterpacks recall — FDA D-0647-2025
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging at the manufacturing site, was detected with presence of a micro-organism. No…
Class IIFDA: OngoingAmerisource Health Services LLC
DrugSep 24, 2025
KIT FOR THE PREPARATION OF TECHNETIUM TC99M MERTIATIDE Kit for the Preparation of Technetium recall — FDA D-0658-2025
Failed Dissolution Specifications-Out of Specification (OOS) observation for sulphate in Sodium Tartrate Dihydrate used for the production of Mertiatide.
Class IIFDA: OngoingSUN PHARMACEUTICAL INDUSTRIES INC
DrugSep 24, 2025
chlorproMAZINE Hydrochloride Tablets, USP, 100 mg, 100 (10x10) blisterpack per carton recall — FDA D-0649-2025
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging at the manufacturing site, was detected with presence of a micro-organism. No…
Class IIFDA: OngoingAmerisource Health Services LLC
DrugSep 24, 2025
chlorproMAZINE Hydrochloride Tablets, USP, 50 mg, 100 (10x10) blisterpacks recall — FDA D-0648-2025
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging at the manufacturing site, was detected with presence of a micro-organism. No…
Class IIFDA: OngoingAmerisource Health Services LLC
DrugSep 24, 2025
chlorproMAZINE Hydrochloride Tablets, USP, 200 mg, 100 (10x10) blisterpack per carton recall — FDA D-0650-2025
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging at the manufacturing site, was detected with presence of a micro-organism. No…
Class IIFDA: OngoingAmerisource Health Services LLC
VehicleSep 23, 2025
BMW relay recall — NHTSA campaign 25V636000
BMW of North America, LLC (BMW) is recalling certain 2019-2021 BMW 330i, 2019-2022 BMW Z4, 2020-2022 BMW 530i, X3, X4, Toyota Supra, 2021-2022 BMW 430i, 430i Convertible, and 2022 BMW 230i…
relayBMW of North America, LLC
VehicleSep 18, 2025
General Motors tank recall — NHTSA campaign 25V619000
General Motors, LLC (GM) is recalling certain 2021 Cadillac Escalade, 2021, 2023-2024 Chevrolet Tahoe, and 2022 and 2024 GMC Yukon vehicles equipped with a 6-cylinder diesel engine. The…
tankGeneral Motors, LLC
Medical DeviceSep 17, 2025
Boston Scientific Encore Advantage Kit, Material Numbers (UPN): 1 recall — FDA Z-2534-2025
The Encore 26 Inflation Device is used with balloon dilation catheters to create and monitor pressure in the balloon and to deflate the balloon. An internal investigation determined that…
Class IIFDA: OngoingBoston Scientific Corporation
Medical DeviceSep 17, 2025
Siemens Healthcare Diagnostics Atellica CH Urinary/Cerebrospinal Fluid Protein (UCFP) recall — FDA Z-2542-2025
Potential for falsely depressed patient, quality control (QC), and/or calibration results or delayed results.
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
Medical DeviceSep 17, 2025
CELSITE BABYPORT SET PUR 4,5F IV USA recall — FDA Z-2528-2025
The potential for minor injury such as damage to the vessel and/or tearing of the vessel wall.
Class IIFDA: OngoingB.Braun Medical S.A.S.
Medical DeviceSep 17, 2025
Fortress Introducer Sheath System recall — FDA Z-2532-2025
Units may have been packaged with an incorrect pouch label, which lists the reference number and unique device identifier of the 4F version of the device, rather than the packaged 6F…
Class IIFDA: OngoingContract Medical International GmbH
Medical DeviceSep 17, 2025
Waldemar Link GmbH & Co. KG LinkSymphoKnee System, Tibial Component, Modular, Symmetric, Sz. recall — FDA Z-2541-2025
Some modular LinkSymphoKnee TiNbN Tibial Components were manufactured with two uncoated security screws, which is incorrect.
Class IIFDA: OngoingWaldemar Link GmbH & Co. KG (Mfg Site)
Medical DeviceSep 17, 2025
Boston Scientific Encore 26 Inflation Device, Material Numbers (UPN): 1 recall — FDA Z-2533-2025
The Encore 26 Inflation Device is used with balloon dilation catheters to create and monitor pressure in the balloon and to deflate the balloon. An internal investigation determined that…
Class IIFDA: OngoingBoston Scientific Corporation
Medical DeviceSep 17, 2025
DJO SURGICAL ALTIVATE REVERSE WEDGE GLENOID REAMER SLEEVE recall — FDA Z-2548-2025
Their is a potential that the reamer may kick or bind up during or immediately prior to use.
Class IIFDA: OngoingEncore Medical, LP
Medical DeviceSep 17, 2025
Merit Medical Systems 10Fore Hemostasis Valve Catalog Number / UDI-DI code: MAPTEN4 / recall — FDA Z-2553-2025
Due to a manufacturing issue involving the silicone quad ring where the ring is deformed or otherwise damaged and may cause a foreign body in the fluid pathway.
Class IIFDA: OngoingMerit Medical Systems, Inc.
Medical DeviceSep 17, 2025
CorNeat EverPatch, REF: 1036295, Permanent Tissue-Integrating Surgical Matrix, 5.0 mm x 6.5 recall — FDA Z-2537-2025
Retroactive; Due to complaints, labeling correction for permanent tissue-integrating surgical matrices to include prevention and management of would dehiscence.
Class IIFDA: OngoingCORNEAT VISION, LTD.
Medical DeviceSep 17, 2025
DJO SURGICAL ALTIVATE REVERSE WEDGE GLENOID REAMER HEAD recall — FDA Z-2546-2025
Their is a potential that the reamer may kick or bind up during or immediately prior to use.
Class IIFDA: OngoingEncore Medical, LP
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Recent recall archives
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September 2026361 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 categoriesOctober 2025455 records · 4 categories