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. 2,577 recalls have been distributed to Ohio in the last 12 months.
Showing 30881–30900 of 55,415 recalls
Recalled Item: InflammaDry(R) AN RPS DIAGNOSTIC SOLUTION Recalled by Quidel Corporation Due...
The Issue: In-house testing revealed the presence of plastic spurs at the tips of some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVID TruCustom PLASTIC BASIN PACK convenience kits Recalled by Avid Medical,...
The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVID TruCustom NEURO PK convenience kits Recalled by Avid Medical, Inc. Due...
The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Pressure Monitoring Extension Line Adapters Extends the pressure line...
The Issue: Identification of small pinholes in a single packaging configuration of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Cardioplegia Adapter with Pressure Port Provides access for a Recalled...
The Issue: Identification of small pinholes in a single packaging configuration of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVID TruCustom LAMINECTOMY PACK convenience kits Recalled by Avid Medical,...
The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVID TruCustom OBSTETRICAL PACK convenience kits Recalled by Avid Medical,...
The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Potassium Phosphate (USP) QS 0.9% Sodium Chloride (USP) 250 mL Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MAN OF STEEL capsules Recalled by Vitility Due to Undeclared Sildenafil
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Paroxetine Extended-Release Tablets USP Recalled by Lupin Pharmaceuticals...
The Issue: Failed Dissolution Specifications: out of specification observed in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: QUELICIN (Succinylcholine Chloride) Injection Recalled by Advanced Pharma...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium Phosphate (USP) QS 0.9% Sodium Chloride (USP) 250 mL Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium Phosphate (USP) QS 0.9% Sodium Chloride (USP) 250 mL Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PALLAS M/MAXIMIS MIS Poly Screw Driver B. Part of MAXIMIS Recalled by...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALLAS M/MAXIMIS 55mm MIS Rod. Part of MAXIMIS Pedicle Screw Recalled by...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALLAS M/MAXIMIS 60mm Curved Rod. Part of MAXIMIS Pedicle Screw Recalled by...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALLAS M/MAXIMIS MIS Screw 6.5 x 40mm. Part of MAXIMIS Recalled by Valorem...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALLAS M/MAXIMIS Poly Screw 6.5 x 45mm. Part of MAXIMIS Recalled by Valorem...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALLAS M/MAXIMIS Ratchet T Handle. Part of MAXIMIS Pedicle Screw Recalled by...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALLAS M/MAXIMIS Poly Screw 6.5 x 50mm. Part of MAXIMIS Recalled by Valorem...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.