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. 1,787 recalls have been distributed to Ohio in the last 12 months.
Showing 45781–45800 of 55,415 recalls
Recalled Item: Kariva (desogestrel/ethinyl estradiol and ethinyl estradiol) Tablets 0.15...
The Issue: Failed Impurities/Degradation Specifications: out of specification impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Velivet (desogestrel and ethinyl estradiol tablets - triphasic regimen)...
The Issue: Failed Impurities/Degradation Specifications: out of specification impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Apri (desogestrel and ethinyl estradiol tablets USP) Recalled by Teva...
The Issue: Failed Impurities/Degradation Specifications: out of specification impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mircette (desogestrel/ethinyl estradiol and ethinyl estradiol) Tablets 0.15...
The Issue: Failed Impurities/Degradation Specifications: out of specification impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brevibloc Premixed Injection Recalled by Baxter Healthcare Corp. Due to...
The Issue: Presence of Particulate Matter: Complaints received of discolored solution...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Non-Mydriatic Auto Fundus Camera. Model AFC-330. An ophthalmic camera for...
The Issue: Image taken by AFC-330 has a white spot which may affect diagnosis or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Paragon Laboratory Management Recalled by McKesson Technologies, Inc. Due to...
The Issue: For Paragon Laboratory Management 12.1 and 12.1.1 releases, if used with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Partial loss of...
The Issue: Partial loss of monitoring with the CARESCAPE Monitor B850, B650 or B450....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T R5 Recalled by Philips Medical Systems, Inc. Due to For some...
The Issue: For some identified Ingenia systems shipped between December 2013 and March...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T Recalled by Philips Medical Systems, Inc. Due to For some...
The Issue: For some identified Ingenia systems shipped between December 2013 and March...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T R5 Recalled by Philips Medical Systems, Inc. Due to For some...
The Issue: For some identified Ingenia systems shipped between December 2013 and March...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T Recalled by Philips Medical Systems, Inc. Due to For some...
The Issue: For some identified Ingenia systems shipped between December 2013 and March...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jody's Recalled by Jody's Inc. Due to Undeclared Colors
The Issue: Undeclared colors Blue #1, Blue #2 and Red #40.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Jody's Recalled by Jody's Inc. Due to Undeclared Colors
The Issue: Undeclared colors Blue #1, Red #3 and Yellow #5.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Jody's Recalled by Jody's Inc. Due to Undeclared Color
The Issue: Undeclared color Red #3 .
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Vita Classic Premium Sliced Smoked Atlantic Nova Salmon Recalled by Vita...
The Issue: This voluntary recall is being initiated due to a positive Listeria...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Captomer-250 [succinic acid (from 250 mg DMSA)] capsules Recalled by Thorne...
The Issue: Marketed Without An Approved NDA/ANDA: Captomer and Captomer-250 are...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Captomer [succinic acid (from 100 mg DMSA)] capsules Recalled by Thorne...
The Issue: Marketed Without An Approved NDA/ANDA: Captomer and Captomer-250 are...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Venlafaxine Hydrochloride Extended-Release Tablets Recalled by Caraco...
The Issue: Failed Dissolution Specifications: Stability results found the product did...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Laceration Kit: W/Needles Recalled by Medical Action Industries Inc Due to...
The Issue: Some of the sterile kits may have incomplete seals which might compromise...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.