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. 2,592 recalls have been distributed to Ohio in the last 12 months.
Showing 24261–24280 of 55,415 recalls
Recalled Item: NxStage PureFlow B Solution Recalled by NxStage Medical, Inc. Due to Mislabeling
The Issue: Certain lots were mislabeled with incorrect product number.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Patagonia Provisions Mellow Curry Savory Seeds Recalled by Patagonia...
The Issue: Products are labeled gluten free but have been found to contain gluten in...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Patagonia Provisions Chipotle Lime Savory Seeds Recalled by Patagonia...
The Issue: Products are labeled gluten free but have been found to contain gluten in...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Patagonia Provisions Classic Barbecue Savory Seeds Recalled by Patagonia...
The Issue: Products are labeled gluten free but have been found to contain gluten in...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Patagonia Provisions Savory Seeds Variety Pack Recalled by Patagonia...
The Issue: Products are labeled gluten free but have been found to contain gluten in...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lamb s Supreme Potato Tater Puffs Recalled by Lamb Weston BSW LLC Due to...
The Issue: Formed Potato Tater Puffs (H30 s), sold as a foodservice item, are recalled...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MaxZero Extension Sets with Needle-less Connector Recalled by Becton...
The Issue: BD has decided to initiate a voluntary recall due to a confirmed complaint...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Neurovascular Recalled by Stryker Neurovascular Due to The firm has...
The Issue: The firm has become aware of a potential problem that their Catheters may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Neurovascular Recalled by Stryker Neurovascular Due to The firm has...
The Issue: The firm has become aware of a potential problem that their Catheters may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProACT Implantation Instrument Set Recalled by Uromedica Inc. Due to...
The Issue: Potential issue with the manufacture and inspection of U-channel sheaths in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quidel Triage TOX Drug Screen Control 1 Kit Box containing Recalled by...
The Issue: Due to an error in the programming of the Control CODE CHIP module for this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pericardiocentesis Catheter Tray Recalled by Cook Inc. Due to Affected...
The Issue: Affected products may have been manufactured with the catheter distal end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q (material 10848280 Recalled by Siemens Medical Solutions USA, Inc...
The Issue: In affected Artis systems the movement of the floating tabletop may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q (material 10848280 Recalled by Siemens Medical Solutions USA, Inc...
The Issue: In affected Artis systems the movement of the floating tabletop may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Zeego (material 10280959) - Product Usage: AXIOM Artis zee Recalled by...
The Issue: In affected Artis systems the movement of the floating tabletop may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pericardiocentesis Catheter Set Recalled by Cook Inc. Due to Affected...
The Issue: Affected products may have been manufactured with the catheter distal end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cepheid Xpert SA Nasal Complete Control Panel (Catalog #8196) UDI: Recalled...
The Issue: Product with incorrect shelf life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Zee (material # 10094135 Recalled by Siemens Medical Solutions USA,...
The Issue: In affected Artis systems the movement of the floating tabletop may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cepheid Xpert MRSA/MRSA NxG Control Panel (Catalog #8195) UDI:...
The Issue: Product with incorrect shelf life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pericardiocentesis Catheter Tray Recalled by Cook Inc. Due to Affected...
The Issue: Affected products may have been manufactured with the catheter distal end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.