Product Recalls in Ohio
Product recalls affecting Ohio — including food, drugs, consumer products, medical devices, and vehicles distributed to Ohio. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,118 recalls have been distributed to Ohio in the last 12 months.
Showing 12981–13000 of 30,087 recalls
Recalled Item: Centurion-Medicine Cup GMC205 GLASS MEDICINE CUP 2 OUNCE STERILE Recalled by...
The Issue: Incomplete seals on the sterile package may compromise the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion-Infant Feeding Kit IFK840 INFANT FEEDING KIT (8 FR X 40 IN)...
The Issue: Incomplete seals on the sterile package may compromise the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion- PT225 PAIN MANAGEMENT TRAY Recalled by Centurion Medical Products...
The Issue: Incomplete seals on the sterile package may compromise the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS Varicella Zoster IgG (VZG) antibody IVD Recalled by bioMerieux, Inc....
The Issue: Two batches of VIDAS Varicella-Zoster IgG (VZG ) may yield an invalid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fast-Cath Trio HEMOSTASIS INTRODUCER Recalled by Abbott Medical Due to...
The Issue: Fast-Cath Trio Hemostasis Introducer devices contained 12F sized dilators...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fast-Cath Hemostasis Introducer Recalled by Abbott Medical Due to Three lots...
The Issue: Three lots of Fast-Cath Hemostasis Introducer devices contained 8F sized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz SE & Co. KG Recalled by Karl Storz Endoscopy Due to The firm has...
The Issue: The firm has become aware that there is a potential that the glass cover at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mazor X Surgical System Positioner Type II Recalled by Medtronic Navigation,...
The Issue: There is a potential for the surgical system to detach from the operational...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker T2 Alpha Delta Strike Plate IMN Instruments - part Recalled by...
The Issue: Instrument can break at the level of the thread when being exposed to high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lunar iDXA Pro/Lunar iDXA Advance (iDXA with enCORE v18) bone densitometer...
The Issue: An issue with the Lunar iDXA control panel may cause the start button to not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lunar iDXA Pro/Lunar iDXA Advance (iDXA with enCORE v17) bone densitometer...
The Issue: An issue with the Lunar iDXA control panel may cause the start button to not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Healon GV PRO 0.85 mL Recalled by Johnson & Johnson Surgical Vision Inc Due...
The Issue: Ophthalmic viscosurgical device may be difficult to remove from the eye,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lunar iDXA bone densitometer Recalled by GE Healthcare, LLC Due to An issue...
The Issue: An issue with the Lunar iDXA control panel may cause the start button to not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lunar iDXA Advance (iDXA with enCORE v16) bone densitometer Recalled by GE...
The Issue: An issue with the Lunar iDXA control panel may cause the start button to not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Cardiopulmonary (MCP)/Getinge ROTAFLOW Drive Recalled by Maquet...
The Issue: A loose ODU plug / Coaxial cable connection may result in fluctuating flow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical convenience trays and kits Recalled by Medical Action Industries,...
The Issue: The kits contain a bottle of saline solution which may exceed the USP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartMate 3 Mobile Power Unit Recalled by Thoratec Corp. Due to Excessive...
The Issue: Excessive static electricity can potentially cause unrecoverable power loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PTS Diagnostics CardioChek Plus Professional Analyzer Recalled by Polymer...
The Issue: One brand of batteries have a small dimensional difference in the negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PTS Diagnostics CardioChek Plus Professional Analyzer Recalled by Polymer...
The Issue: One brand of batteries have a small dimensional difference in the negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioPince Full Core Biopsy Instrument 16ga x 15cm. Recalled by Argon Medical...
The Issue: Incorrect product labeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.