All Recalls

419 recalls found

Date▼	Source	Product	Brand▼	Severity	Units▼
2026-03-05	NHTSA	Tire Sidewall Damage	General Motors, LLC	N/A	826
2026-03-05	NHTSA	Improperly Stripped Wires May Cause Electrical Arcing	Forest River, Inc.	N/A	116
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	Second-Row Seat Backs May Fail to Lock	Toyota Motor Engineering & Manufacturing	N/A	550,007
2026-03-05	NHTSA	Tire Tread May Separate/FMVSS 139	Kumho Tire Co., Inc.	N/A	11,169
2026-03-04	FDA Drug	FDA Recall: Amantadine HCl, Capsules, UPS, 100 mg, 50 Capsules (5 x 10) unit dose, Rx Only, Manufactured for: Av	AvKARE	Class II	N/A
2026-03-04	FDA Device	FDA Recall: Olympus Inner Sheath. Model No. A4741. for endoscopic diagnosis and treatment in gynecological appl	Olympus Corporation of the Americas	Class II	N/A
2026-03-04	FDA Drug	FDA Recall: Vista Gel Hypromellose USP 0.3% w/v, Eye Drops Dry Eye Relief Lubricating Gel, 10 ml. (1/3 fl. oz),	Wizcure Pharmaa Private Limited	Class II	N/A
2026-03-04	FDA Food	FDA Recall: Gerber Arrowroot Biscuits, Net Wt. 5.5 oz. (155g), packaged in a plastic resealable bag with UPC 015	Gerber Products Company dba Nestle Infant Nutrition	Class II	N/A
2026-03-04	FDA Device	FDA Recall: Olympus Resection Sheath; Model No. A2666. Resection sheath for urologic applications.	Olympus Corporation of the Americas	Class II	N/A
2026-03-04	FDA Device	FDA Recall: Brand Name: Reverse Shoulder Prosthesis (RSP) Product Name: RSP STANDARD HUMERAL SOCKET INSERT, 36M	Encore Medical, LP	Class II	N/A
2026-03-04	FDA Drug	FDA Recall: Vista Gonio Eye Lubricant, Hypromellose Ophthalmic Solution USP (Sterile Drops. Dry Eye Relief, 15 m	Wizcure Pharmaa Private Limited	Class II	N/A
2026-03-04	FDA Device	FDA Recall: Olympus Resection Sheath, 8 mm. Model No. A42011A. Resection sheath for gynecological applications.	Olympus Corporation of the Americas	Class II	N/A
2026-03-04	FDA Device	FDA Recall: Campy CVA Medium 100/PK, R01272	Remel, Inc	Class II	N/A
2026-03-04	FDA Device	FDA Recall: Convenience kits containing Tego Connectors: Medline DIALYSIS DRESSING CHANGE SKU EBSI1498 Me	Medline Industries, LP	Class II	N/A
2026-03-04	FDA Device	FDA Recall: Medline Kits containing Tego Connectors: Medline IR Pack, SKU DYNJ67205C Medline NO CATHETER DIALY	Medline Industries, LP	Class II	N/A
2026-03-04	FDA Food	FDA Recall: Yoyo Gummy Tropical Flavor, 2.8 Oz (80g) , Plastic Bag, 24 bags per case	SB FOOD LLC	Class II	N/A
2026-03-04	FDA Drug	FDA Recall: CHNaO Fluorescein Sodium Ophthalmic Strips, USP 1mg, packaged as a) 100-count box, NDC 83851-100-10;	Wizcure Pharmaa Private Limited	Class II	N/A
2026-03-04	FDA Device	FDA Recall: Olympus Resection Sheath, 24 Fr; Model No. A22041A. Resection sheath for urologic applications.	Olympus Corporation of the Americas	Class II	N/A
2026-03-04	FDA Drug	FDA Recall: Agebox iKids-Growth (Night Formula), 60-count bottles, Manufactured Exclusively For: AGEBOX Inc., Wi	Agebox	Class II	N/A
2026-03-04	FDA Food	FDA Recall: Tiki Bar Candy Dark Chocolatey Peanut Butter & Pretzel. Net wt: Approx: 2 oz (57g). UPC 8 55725 0051	J2C Hawaii LLC	Class II	N/A
2026-03-04	FDA Device	FDA Recall: Medline Convenience Kits: 1) NAIL KIT, Model Number: DYKM1528	Medline Industries, LP	Class II	N/A
2026-03-04	FDA Device	FDA Recall: Olympus Resection Sheath, 26 Fr. with Deflecting Obturator; Model No. A22042T. Resection sheath for	Olympus Corporation of the Americas	Class II	N/A
2026-03-04	FDA Food	FDA Recall: Valley Springs Steamed Distilled Water. 1 Gal Net, 128 Fl. Oz. UPC 0 31193-00601 2. Bottled by Va	Valley Springs Artesian Gold, LLC	Class II	N/A

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