All Recalls

418 recalls found

Date▼	Source	Product	Brand▼	Severity	Units▼
2026-03-11	FDA Device	FDA Recall: Brand Name: AESCULAP Product Name: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Model/Catalog Number: F	Aesculap Inc	Class II	N/A
2026-03-11	FDA Device	FDA Recall: Esaote Endocavity ultrasonic probe, Model E 3-12, REF 120000038	ESAOTE S.P.A.	Class II	N/A
2026-03-11	FDA Device	FDA Recall: cobas pro integrated solutions with cobas c 503 analytical units: cobas pro sample supply unit, m	Roche Diagnostics Operations, Inc.	Class II	N/A
2026-03-11	FDA Device	FDA Recall: GE Healthcare Centricity Universal Viewer Zero Footprint Client, Model Numbers: 2110344-039, 211034	GE Healthcare	Class II	N/A
2026-03-11	FDA Device	FDA Recall: CS300 IABP. Software Version CS300 IABP C.01.	Datascope Corp.	Class II	N/A
2026-03-11	FDA Device	FDA Recall: Atellica CH Urine Albumin (UAlb). Material Number: 11537225	Siemens Healthcare Diagnostics, Inc.	Class II	N/A
2026-03-11	FDA Device	FDA Recall: CS100 IABP. Software Version CS100 IABP Q.01.	Datascope Corp.	Class II	N/A
2026-03-11	FDA Device	FDA Recall: Brand Name: B. Braun Product Name: 21GA WINGED INFUSION, SINGLE PK Model/Catalog Number: 7A3842 S	B Braun Medical Inc	Class II	N/A
2026-03-11	FDA Device	FDA Recall: Brand Name: B. Braun Product Name: BBraun Medical 21G X4.4CM Winged INF Model/Catalog Number: 7B30	B Braun Medical Inc	Class II	N/A
2026-03-11	FDA Device	FDA Recall: Brand Name: ShockPulse-SE Lithotripsy System SPL-SR Product Name: ShockPulse-SE Lithotripsy System	Olympus Corporation of the Americas	Class II	N/A
2026-03-11	FDA Device	FDA Recall: Brand Name: STA Liatest Free Protein S Product Name: STA Liatest Free Protein S Model/Catalog Numb	Diagnostica Stago, Inc.	Class II	N/A
2026-03-11	FDA Device	FDA Recall: Gelsoft Plus, REF: 635024PE, 631514PE, 631222PE, 633008PE, 633010PE, 633007PE, 636010PE, 632522PE, 6	Vascutek, Ltd.	Class II	N/A
2026-03-11	FDA Device	FDA Recall: Brand Name: Olympus ShockPulse-SE Lithotripsy System with Generator Product Name: ShockPulse-SE Lit	Olympus Corporation of the Americas	Class II	N/A
2026-03-11	FDA Device	FDA Recall: Brand Name: HiResolution Bionic Ear System Product Name: Sky CI M90 Sound Processor Model/Catalog	Advanced Bionics, LLC	Class II	N/A
2026-03-11	FDA Device	FDA Recall: Brand Name: ShockPulse-SE Lithotripsy System SPL-S Product Name: ShockPulse-SE Lithotripsy System -	Olympus Corporation of the Americas	Class II	N/A
2026-03-09	NHTSA	Incorrectly Installed Cable May Prevent Door from Opening	Mercedes-Benz USA, LLC	N/A	10
2026-03-09	NHTSA	Electrical Distribution Panel Not Properly Grounded	Forest River, Inc.	N/A	27
2026-03-09	NHTSA	Rear Seat Belt Buckle May Not Latch	Kia America, Inc.	N/A	14,870
2026-03-09	NHTSA	Spare Tire Carrier May Detach	ESCAPE TRAILER INDUSTRIES LTD.	N/A	324
2026-03-09	NHTSA	Solar Panel May Detach	Pebble Mobility Inc.	N/A	22
2026-03-05	NHTSA	High Voltage Battery May Fail and Cause Fire	Webasto Thermo & Comfort NA, INC	N/A	89
2026-03-05	NHTSA	Engine Stall Due to Disabled Rear Fuel Pump	General Motors, LLC	N/A	11,807
2026-03-05	NHTSA	Tire Tread May Separate/FMVSS 139	Kumho Tire Co., Inc.	N/A	11,169
2026-03-05	CPSC	HALO Dream Recalls Magic Sleepsuits Due to Choking Hazard	-	N/A	N/A
2026-03-05	CPSC	Tomum Minoxidil Hair Serum Spray Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging; Distributed by Belleka	-	N/A	N/A

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