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. 2,561 recalls have been distributed to Ohio in the last 12 months.
Showing 33181–33200 of 55,415 recalls
Recalled Item: Fem IM Nail 16mmdx44cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fem IM Nail 16mmdx42cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Por fullct fem st 15x200mm Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mammotome Revolve Dual Vacuum Assist Biopsy System The device is Recalled by...
The Issue: The device did not have Revolve Stereo Probe labeling, no product code...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fem IM Nail 15mmdx48cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Handpiece Sheaths Recalled by ConMed Corporation Due to For over a...
The Issue: For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Welch Allyn ProBP 2400 Digital Blood Pressure Device #2400 Recalled by Welch...
The Issue: A defective electrical component in the battery charging circuit in two lots...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Axiom Artis fluoroscopic x-ray system Recalled by Siemens Medical Solutions...
The Issue: A gap in the housing of the wireless foot switch could potentially result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDTECH ROSA Brain 3.0 The device is intended for the Recalled by Zimmer...
The Issue: Unapproved change made by the supplier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDTECH ROSA Spine 1.0.2 The device is intended for the Recalled by Zimmer...
The Issue: Unapproved change made by the supplier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q and Q.Zen fluoroscopic x-ray system Recalled by Siemens Medical...
The Issue: A gap in the housing of the wireless foot switch could potentially result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Zee and Zeego fluoroscopic x-ray system Recalled by Siemens Medical...
The Issue: A gap in the housing of the wireless foot switch could potentially result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liebel-Flarsheim Direct Digital Imaging System (DDIS) Liebel-Flarsheim...
The Issue: Software issue. The difference between the display and dosimeter readings In...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liebel-Flarsheim Hydra Vision Urology X-Ray System (DR) Liebel-Flarsheim...
The Issue: Software issue. The difference between the display and dosimeter readings In...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Meijer Caesar Salad labeled as Meijer Greek Salad Recalled by Meijer Inc Due...
The Issue: Meijer announced it is recalling a recent shipment of its pre-made Caesar...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fusia Asian Aspirations Szechuan Stir Fry Recalled by Versa Marketing Due to...
The Issue: Product was tested and found positive for Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Trader Joe's Organic Unsweetened Apple Sauce Recalled by Manzana Products...
The Issue: Manzana Products Co. is initiating a recall of three varieties of apple...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Trader Joe's First Crush Unsweetened Gravenstein Apple Sauce Recalled by...
The Issue: Manzana Products Co. is initiating a recall of three varieties of apple...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Trader Joes Imported English Authentic Lemon Curd Recalled by Trader Joes...
The Issue: Trader Joe's Co. is recalling the Lemon Curd because it contains undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Trader Joe's All Natural Unsweetened Apple Sauce Recalled by Manzana...
The Issue: Manzana Products Co. is initiating a recall of three varieties of apple...
Recommended Action: Do not consume. Return to store for a refund or discard.