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. 2,806 recalls have been distributed to Ohio in the last 12 months.
Showing 1641–1660 of 55,415 recalls
Recalled Item: i-STAT CG4+ cartridge (white). List Number: 03P85-25. Recalled by Abbott...
The Issue: Lack of a 510(k) premarket clearance for the i-STAT CG4+ cartridge to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frontier Devices Recalled by Folsom Metal Products, Inc. Due to Labeling...
The Issue: Labeling includes shelf life that has not been validated.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT CG8+ cartridge. List Number: 03P88-25. 510(k) numbers: K894914...
The Issue: Lack of a 510(k) premarket clearance for the i-STAT CG8+, EG7+ and EG6+...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frontier Devices Recalled by Folsom Metal Products, Inc. Due to Labeling...
The Issue: Labeling includes shelf life that has not been validated.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frontier Devices Recalled by Folsom Metal Products, Inc. Due to Labeling...
The Issue: Labeling includes shelf life that has not been validated.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frontier Devices Recalled by Folsom Metal Products, Inc. Due to Labeling...
The Issue: Labeling includes shelf life that has not been validated.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT EG7+ cartridge. List Number: 03P76-25. Recalled by Abbott Point Of...
The Issue: Lack of a 510(k) premarket clearance for the i-STAT CG8+, EG7+ and EG6+...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hostess Ding Dongs CHOCOLATE CAKE WITH CREAMY FILLING 2.55 oz Recalled by...
The Issue: Mold. The firm noticed an increase in customer complaints. They conducted a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sulfamethoxazole and Trimethoprim Tablets Recalled by Northwind...
The Issue: Presence of a Foreign Substance: A specific lot of auxiliary polyester coil,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acetaminophen Injection 1000 mg/100 mL (10 mg/mL) Recalled by Baxter...
The Issue: Discoloration
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carvedilol Tablets USP Recalled by The Harvard Drug Group LLC dba Major...
The Issue: CGMP Deviations: Results for N-Nitroso Carvedilol Impurity-1 (NNCI) impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MST ArcDUO 9mm Recalled by MicroSurgical Technology Inc Due to An ophthalmic...
The Issue: An ophthalmic knife has a suction set (not direct patient-contacting), which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Automated Impella Controller (AIC) with the below brands and product...
The Issue: Specific Automated Impella Controllers (AICs) that have a Pump Driver...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hershey s Ice Cream Recalled by HERSHEY CREAMERY CO. Due to Product tested...
The Issue: Product tested elevated coliform counts during routine testing
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: READYPREP PVP Recalled by Medline Industries, LP Due to Subpotent drug
The Issue: Subpotent drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dextroamphetamine Saccharate Recalled by Lannett Company Inc. Due to...
The Issue: Presence of Foreign Tablet/Capsule: Two (2) bottles labeled as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: Vacuette Product Name: 8 ml CAT Serum Separator Recalled by...
The Issue: Some of the Vacuette¿ CAT Serum Separator Clot Activator tubes were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by B BRAUN MEDICAL INC Due to...
The Issue: Presence of Particulate Matter.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: chlorproMAZINE Hydrochloride Tablets Recalled by Amneal Pharmaceuticals, LLC...
The Issue: Presence of a foreign substance.A specific lot of auxiliary polyester coil,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: chlorproMAZINE Hydrochloride Tablets Recalled by Amneal Pharmaceuticals, LLC...
The Issue: Presence of a foreign substance.A specific lot of auxiliary polyester coil,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.