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. 2,542 recalls have been distributed to Ohio in the last 12 months.
Showing 38421–38440 of 55,415 recalls
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magnesium Sulfate in Water for Injection Recalled by Hospira Inc. Due to...
The Issue: Labeling: Incorrect Barcode: Primary bag labeling may be mislabeled with the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bromfenac Ophthalmic Solution 0.09% Recalled by Mayne Pharma Usa Due to Lack...
The Issue: Lack of Assurance of Sterility: Failed preservative effectiveness test
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: T-piece Nebulizer with in-line connectors Recalled by Salter Labs Due to...
The Issue: Reports that the T-piece does not fit on the nebulizer.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InVision-Plus CS Needleless IV Connector Recalled by Rymed Technologies, LLC...
The Issue: Potential for the female luer component of the InVision-Plus IV connector to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InVision-Plus and InVision-Plus Junior Needleless IV Connector Recalled by...
The Issue: Potential for the female luer component of the InVision-Plus IV connector to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue Measurement Module X1 Model: M3001A Recalled by Philips...
The Issue: The ST elevation alarm on the Patient Monitor or standalone X2 Measurement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue Module Measurement X2 Model: M3002A Recalled by Philips...
The Issue: The ST elevation alarm on the Patient Monitor or standalone X2 Measurement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toomey Syringe 70cc Syringe with Catheter Tip and Luer Tip Adapters Recalled...
The Issue: Report by a customer of an open package seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ottobock Modular Polycentric EBS Knee Joint 3R60 Recalled by Otto Bock...
The Issue: Otto Bock HealthCare GmbH is recalling Modular Polycentric EBS Knee Joint...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baked Recalled by Giant Eagle, Inc. Due to Undeclared Walnuts
The Issue: Product contained undeclared walnuts
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: NORepinephrine Bitartrate Recalled by Pharmedium Services, LLC Due to...
The Issue: Subpotent Drug; confirmed results by FDA analysis after customer complaints...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NORepinephrine Bitartrate Recalled by Pharmedium Services, LLC Due to...
The Issue: Subpotent Drug; confirmed results by FDA analysis after customer complaints...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Candesartan Cilexetil Tablets Recalled by Sandoz Inc Due to Failed...
The Issue: Failed Impurities/Degradation Specifications; 9 month stability timepoint
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Little Temptations Sour Strawberries Net Wt. 7.5 oz (213g) Packed Recalled...
The Issue: Sour strawberries contain undeclared FD&C Blue #1 and Yellow #5.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CORDIS AVANTI + CATHETER SHEATH INTRODUCER SYSTEM The product includes...
The Issue: Incorrect cannula of the sheath introducer (smaller than intended).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: This reagent is for in vitro diagnostic use. Pax-5 (1EW) Recalled by Leica...
The Issue: The Bond" Polymer Detection and Novolink" Polymer Detection System may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PharmaCaribe PulmoSal 7% Sodium chloride Recalled by Pharmacaribe llc Due to...
The Issue: Vials were labeled as USP 7% Hypertonic saline instead of PulmoSal 7% (pH+)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.