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. 2,484 recalls have been distributed to Ohio in the last 12 months.
Showing 55181–55200 of 55,415 recalls
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to When performing a...
The Issue: When performing a secondary capture generated from GSI Viewer, the header...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boule Con-Diff Hematology Control For in vitro diagnostic use as Recalled by...
The Issue: Clinical Diagnostic Solutions, Inc. in Plantation, FL recalled Boule Con...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boule Con-Diff Hematology Control For in vitro diagnostic use as Recalled by...
The Issue: Clinical Diagnostic Solutions, Inc. in Plantation, FL recalled Boule Con...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boule Con-Diff Hematology Control For in vitro diagnostic use as Recalled by...
The Issue: Clinical Diagnostic Solutions, Inc. in Plantation, FL recalled Boule Con...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Reliance AL Implant Blocker (Various sizes) The SLIDE Implant...
The Issue: Stryker Spine has received six reports regarding the breakage of one or more...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbiq Two Channel Infuser Recalled by Hospira Inc. Due to May go to a white...
The Issue: May go to a white screen due to a problem with the SOM2 module. A white...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbiq One Channel Infuser Recalled by Hospira Inc. Due to May go to a white...
The Issue: May go to a white screen due to a problem with the SOM2 module. A white...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CONCENTRATED SODIUM CHLORIDE INJECTION Recalled by Luitpold Pharmaceuticals,...
The Issue: Presence of Particulate Matter: In the course of inspecting retention...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LANX Recalled by Biomet Spine LLC. Due to Biomet Spine, LLC. announces...
The Issue: Biomet Spine, LLC. announces voluntary recall of Durango Anchored ALIF Plate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: The DoseRight feature suggest a mAs based on the measured patient size, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Imagecast PACS is an image management system intended to be Recalled by Ge...
The Issue: In Imagecast PACS versions prior to 3.6.51.01, the estimated magnification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ****** 3mm Diamond Ball. Used for cutting and shaping bone. Recalled by The...
The Issue: Due to three batches of product may have diamond grit size larger than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 Computed Tomography X-Ray System Recalled by Philips Medical...
The Issue: Multiple software defects which could impact the performance or reliability...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Custom Cardioplegia Delivery Set- Catalog Number:165720 and Catalog...
The Issue: Defect in the luer connector can compromise the seal on the female side of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Custom Integrated Cardioplegia Delivery Set-LINE FOR 15501/16015/5852...
The Issue: Defect in the luer connector can compromise the seal on the female side of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Custom Cardioplegia Delivery Set - Heat Exchanger Cardiopulmonary...
The Issue: Defect in the luer connector can compromise the seal on the female side of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Cardioplegia Delivery Set- Item Number: 16130 Product Usage: The...
The Issue: Defect in the luer connector can compromise the seal on the female side of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Custom Cardiovascular and Perfusion Procedure Kits Catalog Codes:...
The Issue: Defect in the luer connector can compromise the seal on the female side of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Custom Cardioplegia Delivery Sets Catalog Code: 204880 Product Usage:...
The Issue: Defect in the luer connector can compromise the seal on the female side of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The pizza dough shells come in 5 lb. brown cardboard boxes Recalled by Ron's...
The Issue: There is no labeling on the product, and the product contains the allergen,...
Recommended Action: Do not consume. Return to store for a refund or discard.