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. 2,597 recalls have been distributed to Ohio in the last 12 months.
Showing 22381–22400 of 55,415 recalls
Recalled Item: Grab n Go Opti series VIPR system Model # PRX-9627 Recalled by Western /...
The Issue: Limited access to flow settings as a result of the control knob having been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XP-XP Tibial Tray - Interlok 69 mm Item # 195754 Recalled by Zimmer Biomet,...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grab n Go Opti series VIPR system Model # PRX-9632 Recalled by Western /...
The Issue: Limited access to flow settings as a result of the control knob having been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XP-XP Tibial Tray - Interlok 67 mm Item # 195753 Recalled by Zimmer Biomet,...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XP-XP Tibial Tray - Interlok 79 mm Item # 195758 Recalled by Zimmer Biomet,...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XP-XP Tibial Tray - Interlok 65 mm Item # 195752 Recalled by Zimmer Biomet,...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XP-CR Tibial Tray - Interlok 83 mm Item # 195277 Recalled by Zimmer Biomet,...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard XP Tibial Tray 67 mm Item # 195247 Recalled by Zimmer Biomet, Inc....
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XP-CR Tibial Tray - Porous Plasma 91 mm Item # 195291 Recalled by Zimmer...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grab n Go Opti series VIPR system Model # PRX-9653 Recalled by Western /...
The Issue: Limited access to flow settings as a result of the control knob having been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquilex Fluid Control System component: Bag deflector Recalled by WOM World...
The Issue: The deficit displayed by the pump can differ from the real deficit, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM anti-CCP IgG (aCCP) Assay Siemens Material Number: 10732998...
The Issue: Atellica IM anti-CCP IgG (aCCP) Test Definition (TDef) Mitigation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Conquest 40 PTA Dilation Catheter Recalled by Bard Peripheral Vascular...
The Issue: The catheter packaging incorrectly listed the balloon size as 8mm X 20mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RELPAX (eletriptan HBr) tablets Recalled by Pfizer Inc. Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Products: contamination with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metalogix Slotted 90 Tubular Wrench x 10mm LOT A29618A Recalled by New...
The Issue: Due to manufacturing processing error, wrench causing stripping when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AssayTip/AssayCup Tray-used on the cobas e 801 module which is Recalled by...
The Issue: AssayTips part of the AssayTip/AssayCup Tray Tips used on the cobas e 801...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXACTAMED Oral Dispensers Recalled by Baxter Healthcare Corporation Due to...
The Issue: Exactamed 5 mL Oral Dispenser Pharmacy Packs may contain both 5 mL and 3 mL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STRATAFIX Spiral PDS Plus Violet 27 (70cm) CTX Needle Product Recalled by...
The Issue: The product does not meet certain internal strength testing specifications.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STRATAFIX Spiral PDS Plus Violet 18 (45cm) CT-1 Needle Product Recalled by...
The Issue: The product does not meet certain internal strength testing specifications.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S-GLUTATHIONE 200MG/3ML (PF) INHALATION SOLN Recalled by First Royal Care...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.