All Recalls

2227 recalls found

Date▼	Source	Product	Brand▼	Severity	Units▼
2026-06-24	NHTSA	Printed Circuit Board May Overheat	Airstream, Inc.	N/A	303
2026-06-24	NHTSA	Instrument Panel Display Failure/FMVSS 101	Hyundai Motor America	N/A	96,310
2026-06-23	NHTSA	Incorrect Wheel Rim Width on VIN Label/FMVSS 120	Indian Motorcycle Company	N/A	392
2026-06-23	NHTSA	Improperly Tightened Steering Gear Assembly Nut	General Motors, LLC	N/A	26,541
2026-06-23	NHTSA	Headlight May Fail	Piaggio Group Americas, Inc.	N/A	112
2026-06-23	NHTSA	Electrical Shock from Mislabeled Circuit	Forest River, Inc.	N/A	1,824
2026-06-22	NHTSA	Touch Screen Display May Fail	Farber Specialty Vehicles	N/A	3
2026-06-22	NHTSA	Printed Circuit Board May Overheat	Airxcel, Inc.	N/A	5,021
2026-06-18	NHTSA	Loss of Drive Power	Toyota Motor Engineering & Manufacturing	N/A	20,991
2026-06-17	FDA Device	FDA Recall: Siemens Dimension Tacrolimus Flex Reagent Cartridge (TAC), REF DF207, SMN 10700795; enzyme immunoass	Siemens Healthcare Diagnostics, Inc.	Class II	N/A
2026-06-17	FDA Device	FDA Recall: Allia IGS 5 Pulse angiographic X-ray system	GE Medical Systems, LLC	Class II	N/A
2026-06-17	FDA Device	FDA Recall: NeoSpan¿ SuperElastic Compression Staple w/Instruments Catalog Number and Product Name T50 SN010	In2bones USA, LLC	Class II	N/A
2026-06-17	FDA Device	FDA Recall: SD LTM 64 PLUS, EEG Amplifier/recorder, Model/Catalog Number: SD LTM 64 PLUS, Software Version: firm	Micromed S.p.A.	Class II	N/A
2026-06-17	FDA Device	FDA Recall: TDC VELOCE", 27G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT27, 9311.27G01, 9311.27	D.O.R.C. Dutch Opthalmic Research Center Intl B.V.	Class II	N/A
2026-06-17	NHTSA	Alternator Pulley Failure May Cause Power Brakes and Power Steering Loss	Storyteller Overland	N/A	82
2026-06-17	FDA Drug	FDA Recall: Minocycline Hydrochloride Extended-Release Tablets, USP, 115 mg, 30-count bottle, Rx Only, Manufactu	Ascend Laboratories, LLC	Class II	N/A
2026-06-17	FDA Drug	FDA Recall: Primidone Tablets, USP, 50 mg, 100 Tablets per Bottle, Rx only, Manufactured by: Amneal Pharmaceutic	Amneal Pharmaceuticals, LLC	Class III	N/A
2026-06-17	FDA Food	FDA Recall: Individual Unit Label (both lid and front of cup): Whole Foods Market Kitchens Minestrone Soup, VEGE	Kettle Cuisine, LLC	Class I	N/A
2026-06-17	FDA Device	FDA Recall: TDC VELOCE", 25G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT25, 9311.25G01, 9311.25	D.O.R.C. Dutch Opthalmic Research Center Intl B.V.	Class II	N/A
2026-06-17	FDA Device	FDA Recall: Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx40mm Model/Catalog Number: CND0840	INSPIREMD Inc	Class II	N/A
2026-06-17	FDA Drug	FDA Recall: DOXOrubin Hydrochloride Liposome injection, 50 mg/25 mL (2mg/mL), 25 mL single-dose vials, Sterile,	SUN PHARMACEUTICAL INDUSTRIES INC	Class I	N/A
2026-06-17	FDA Drug	FDA Recall: Duloxetine Delayed-Release Capsules, USP, 30mg, 1000 Capsule bottles, Rx only, Manufactured. by: Tow	Breckenridge Pharmaceutical, Inc.	Class II	N/A
2026-06-17	FDA Device	FDA Recall: Allia Moveo angiographic X-ray system	GE Medical Systems, LLC	Class II	N/A
2026-06-17	FDA Device	FDA Recall: Allia IGS 3 Pulse angiographic X-ray system	GE Medical Systems, LLC	Class II	N/A
2026-06-17	FDA Device	FDA Recall: Mahurkar Elite PASS Trays; Description (Product Number/CFN): 12 FR x 13cm Acute Dual Lumen Cathete	Mozarc Medical US LLC	Class II	N/A

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