DrugNov 26, 2025
NIACIN Extended-Release Tablets, USP, 1,000 mg, 90 tablets per bottle recall — FDA D-0158-2026
Failed Dissolution Specifications
Class IIFDA: OngoingGolden State Medical Supply Inc.
Latest records
Latest recalls — page 139
The newest recall records with useful source details are listed here.
DrugNov 26, 2025
DermaRite Industries Renew PeriProtect, Zinc Oxide 12%, Dimethicone 1%, 113g (4 oz.) per recall — FDA D-0174-2026
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Class IIFDA: OngoingDermaRite Industries, LLC
DrugNov 26, 2025
DermaRite Industries PeriGuard Ointment, Petrolatum 49.9% recall — FDA D-0173-2026
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Class IIFDA: OngoingDermaRite Industries, LLC
DrugNov 26, 2025
DermaRite Industries DermaMed Ointment, Skin Protectant, Aluminum Hydroxide Gel 2%, Net Wt. recall — FDA D-0164-2026
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Class IIFDA: OngoingDermaRite Industries, LLC
DrugNov 26, 2025
DermaRite Industries PeriGiene, Health Care Antiseptic, Chloroxylenol 0.5%, 222mL recall — FDA D-0172-2026
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Class IIFDA: OngoingDermaRite Industries, LLC
DrugNov 26, 2025
DermaRite Industries DermaSarra, Camphor 0.5%, External Analgesic, 222 mL (7.5 fl. oz.) per recall — FDA D-0165-2026
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Class IIFDA: OngoingDermaRite Industries, LLC
DrugNov 26, 2025
DermaRite Industries DermaFungal, Antifungal Cream with 2% Miconazole Nitrate recall — FDA D-0162-2026
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Class IIFDA: OngoingDermaRite Industries, LLC
DrugNov 26, 2025
DermaRite Industries KleenFoam Antimicrobial Foam Soap, Chloroxylenol 0.5%, 34 FL OZ recall — FDA D-0168-2026
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Class IIFDA: OngoingDermaRite Industries, LLC
DrugNov 26, 2025
DermaRite Industries Lantiseptic, Skin Protectant, Lanolin USP 30% recall — FDA D-0170-2026
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Class IIFDA: OngoingDermaRite Industries, LLC
VehicleNov 25, 2025
Volvo Car USA critical fasteners recall — NHTSA campaign 25V818000
Volvo Car USA, LLC (Volvo) is recalling certain 2026 XC60MHEV, 2018 and 2025 XC60 vehicles. The front seat bolts may have been improperly tightened, resulting in loose bolts.
critical fastenersVolvo Car USA, LLC
VehicleNov 25, 2025
General Motors owners/service/other manual recall — NHTSA campaign 25V815000
General Motors, LLC (GM) is recalling certain 2026 Chevrolet Silverado 1500, 2500, and 3500 vehicles. These vehicles may not have received an owner's manual during production. As such,…
owners/service/other manualGeneral Motors, LLC
VehicleNov 21, 2025
Sentra windshield recall — NHTSA campaign 25V807000
Nissan North America, Inc. (Nissan) is recalling certain 2025 Sentra vehicles. The windshield glass may have visible air bubbles, which can obscure the driver's visibility. As such, these…
windshieldNissan North America, Inc.
VehicleNov 21, 2025
Hyundai Motor display function recall — NHTSA campaign 25V808000
Hyundai Motor America (Hyundai) is recalling certain 2024-2025 Santa Fe and Santa Fe Hybrid vehicles. The rearview camera may not have been installed properly, which can damage the wiring…
display functionHyundai Motor America
VehicleNov 21, 2025
Hyundai Motor curtain recall — NHTSA campaign 25V809000
Hyundai Motor America (Hyundai) is recalling certain 2025 Tucson, 2025-2026 Santa Cruz, Santa Fe, Santa Fe Hybrid, and 2026 Genesis GV70 vehicles. The side curtain air bags may not have…
curtainHyundai Motor America
Medical DeviceNov 19, 2025
Medline Industries Anesthesia circuit kit recall — FDA Z-0449-2026
Firm received multiple complaints of anesthesia circuit leaks due to cracks in the 120" expandable tubing. Cracks and resulting leaks may lead to hypoxia, hypoventilation, and inadequate…
Class IFDA: OngoingMedline Industries, LP
Medical DeviceNov 19, 2025
Philips Medical Systems DMC GmbH DigitalDiagnost 4 (1) High Performance, (2) Flex/Value recall — FDA Z-0464-2026
Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/physical…
Class IIFDA: OngoingPhilips Medical Systems DMC GmbH
Medical DeviceNov 19, 2025
Stryker Sustainability Solutions HARMONIC FOCUS Shears + Adaptive Tissue Technology, 9 cm recall — FDA Z-0490-2026
Due to manufacturing issue, reprocessed shears, may become stuck in the "on position" resulting in continuous activation.
Class IIFDA: OngoingStryker Sustainability Solutions
Medical DeviceNov 19, 2025
Medline Renewal LigaSure Maryland Jaw Sealer/Divider Nano Coated, Compatible with FT10 recall — FDA Z-0475-2026
Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodged.
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceNov 19, 2025
Siemens Medical Solutions USA MAGNETOM Cima.X Upgrade recall — FDA Z-0431-2026
There is a potential for an ice blockage to form or currently exist within the primary and/or the auxiliary venting paths of the magnet helium containment venting system. In the event of a…
Class IFDA: OngoingSiemens Medical Solutions USA, Inc.
Medical DeviceNov 19, 2025
Medline Renewal LigaSure Maryland Jaw Sealer/Divider NanoCoated, Compatible w/FT10 37 cm recall — FDA Z-0476-2026
Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodged.
Class IIFDA: OngoingMedline Industries, LP
Medical DeviceNov 19, 2025
SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION Ceiling Type X-Ray Tube Support Models CH-200 recall — FDA Z-0499-2026
Due to an issue (potential breakage) with the shaft for the mounting of the X-ray tube assembly that could potentially result assembly coming off the rotating shaft.
Class IIFDA: OngoingSHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION
Medical DeviceNov 19, 2025
Olympus Single Use Electrosurgical Snare SD-400 Single Use Electrosurgical Snare recall — FDA Z-0482-2026
Sterility compromised from small holes that may occur during packaging of the device pouches into the shelf carton and/or during transportation of the shelf carton.
Class IIFDA: OngoingOlympus Corporation of the Americas
Medical DeviceNov 19, 2025
Becton Dickinson & Co BD Kiestra" Isolate Suspension Cuvette Array recall — FDA Z-0484-2026
The 2D barcodes on these cuvettes contain formatting errors that prevent the analyzing system from correctly reading the expiration date. As a result, the instrument enters an error state…
Class IIFDA: OngoingBecton Dickinson & Co.
Medical DeviceNov 19, 2025
Medline Renewal LigaSure Impact Curved Large Jaw Sealer/Divider, Compatible with FT10 recall — FDA Z-0468-2026
Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodged.
Class IIFDA: OngoingMedline Industries, LP
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
September 2026300 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