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. 1,127 recalls have been distributed to Ohio in the last 12 months.
Showing 11161–11180 of 55,415 recalls
Recalled Item: Rifampin Capsules USP Recalled by Lupin Pharmaceuticals Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Failure observed in related...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: By Heart Whole Nutrition Infant Formula Recalled by ByHeart, INC. Due to...
The Issue: Infant formula potentially contaminated with Cronobacter sakazakii
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CADD Administration Set Recalled by Smiths Medical ASD Inc. Due to There are...
The Issue: There are two potential issues with CADD Infusion System Infusion Sets: (1)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD Administration Set Recalled by Smiths Medical ASD Inc. Due to There are...
The Issue: There are two potential issues with CADD Infusion System Infusion Sets: (1)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD Administration Set Recalled by Smiths Medical ASD Inc. Due to There are...
The Issue: There are two potential issues with CADD Infusion System Infusion Sets: (1)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD Administration Set Recalled by Smiths Medical ASD Inc. Due to There are...
The Issue: There are two potential issues with CADD Infusion System Infusion Sets: (1)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD Administration Set Recalled by Smiths Medical ASD Inc. Due to There are...
The Issue: There are two potential issues with CADD Infusion System Infusion Sets: (1)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcohol Antiseptic 80% Topical Solution Hand Sanitizer Recalled by NCH Life...
The Issue: CGMP Deviations: Impurities of acetal and acetaldehyde were discovered in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thiamine Hydrochloride 200 mg/2mL (100mg/mL) Recalled by McGuff Compounding...
The Issue: Presence of Particulate Matter: Presence of foreign substances were reported...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thiamine Hydrochloride 3000 mg/30 mL (100mg/mL) Recalled by McGuff...
The Issue: Presence of Particulate Matter: Presence of foreign substances were reported...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Slick Set Cuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...
The Issue: Potential for pilot balloon non-inflation or cuff non-deflation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotracheal Tube labeled as the following: a. Endotracheal Tube oral/nasal...
The Issue: Potential for pilot balloon non-inflation or cuff non-deflation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RadiaLux Lighted Retractor (Pink) Recalled by Medtronic Navigation, Inc. Due...
The Issue: Defect in sterile pouch seal, incomplete seal, of lighted Retractors,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Detect Covid-19 Test Product/Model Number: 21205 Recalled by Detect...
The Issue: There is an increased chance that the tests from affected lots may give...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotracheal Tube labeled as the following: a. Flexi-Set Cuffed Endotracheal...
The Issue: Potential for pilot balloon non-inflation or cuff non-deflation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical convenience kits labeled as: MEDLINE PAIN TRAY Recalled by MEDLINE...
The Issue: The recall is due to the perforated bag not allowing for outside of the kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 13.5Fr High Flow Dual Lumen Acute Dialysis Catheter Recalled by...
The Issue: There is a potential leaking condition within the hub of affected devices,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical convenience kits labeled as: MEDLINE BREAST BIOPSY KIT Recalled by...
The Issue: The recall is due to the perforated bag not allowing for outside of the kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical convenience kits labeled as: MEDLINE SHOULDER SUSPENSION I-LF...
The Issue: The recall is due to the perforated bag not allowing for outside of the kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7.5 cm Large Rotating Craniotome Attachment. Use with XMax¿ Recalled by The...
The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.