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. 2,635 recalls have been distributed to Ohio in the last 12 months.
Showing 18681–18700 of 55,415 recalls
Recalled Item: DISCOVERY ULTRA Advanced Staining System (RUO-Research Use Only) Material...
The Issue: Potential for Fluid leaks within the instruments, creating an electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BellaTek Encode Defin3DPMSERitive Abutments-3D Printed Model Numbers:...
The Issue: Hex of the BellaTek Encode Definitive Abutments was misaligned by 30 degrees...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pediatric Nephrostomy Stent Set Recalled by Cook Inc. Due to The indwell...
The Issue: The indwell time for the Percutaneous Neonatal Pigtail Nephrostomy Set and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Neonatal Pigtail Nephrostomy Set Recalled by Cook Inc. Due to...
The Issue: The indwell time for the Percutaneous Neonatal Pigtail Nephrostomy Set and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasound Navigation Software 1.0 and Ultrasound Integration Software for...
The Issue: Brainlab Ultrasound Navigation Software does not support the modification of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CERTAIN BELLATEK TITANIUM ABUTMENT 5.0MM Number: IEDAT5 Recalled by Biomet...
The Issue: Hex of the BellaTek Encode Definitive Abutments was misaligned by 30 degrees...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CERTAIN BELLATEK TIN ABUTMENT 4.1MM Number: IEDAN4 Recalled by Biomet 3i,...
The Issue: Hex of the BellaTek Encode Definitive Abutments was misaligned by 30 degrees...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CERTAIN BELLATEK TITANIUM ABUTMENT 4.1MM Number: IEDAT4 Recalled by Biomet...
The Issue: Hex of the BellaTek Encode Definitive Abutments was misaligned by 30 degrees...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BenchMark ULTRA Advanced Staining System (IVD)- Material Number: 05342716001...
The Issue: Potential for Fluid leaks within the instruments, creating an electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CERTAIN BELLATEK TITANIUM ABUTMENT 6.0MM Number: IEDAT6 Recalled by Biomet...
The Issue: Hex of the BellaTek Encode Definitive Abutments was misaligned by 30 degrees...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PermaFlo Flowable Composite 948 Shade: A2 - Product Usage: Recalled by...
The Issue: Due to a potential manufacturing issue (cross contamination), composite is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CERTAIN BELLATEK TIN ABUTMENT 5.0MM Number: IEDAN5 Recalled by Biomet 3i,...
The Issue: Hex of the BellaTek Encode Definitive Abutments was misaligned by 30 degrees...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Medical Systems Corporation (OMSC) Evis Exera II Bronchovideoscope...
The Issue: The BF-Q180 bronchoscope is being recalled because it does not have a 510(k)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 365 Whole Foods Market Organic Reduced fat &Sodium Popcorn Recalled by EAGLE...
The Issue: Foreign material, pieces of glass may be in the product
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 365 Everyday Value Organic Classic Salted Popcorn Recalled by EAGLE FAMILY...
The Issue: Foreign material, pieces of glass may be in the product
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nice! Organic White Cheddar Popcorn Recalled by EAGLE FAMILY FOODS GROUP LLC...
The Issue: Foreign material, pieces of glass may be in the product
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cretors Organic Extra Virgin Olive Oil Popcorn Recalled by EAGLE FAMILY...
The Issue: Foreign material, pieces of glass may be in the product
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 365 Whole Foods Market Organic White Cheddar Popcorn Recalled by EAGLE...
The Issue: Foreign material, pieces of glass may be in the product
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nature's Promise Organic Lightly Salted Popcorn Recalled by EAGLE FAMILY...
The Issue: Foreign material, pieces of glass may be in the product
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Organic Yellow Popcorn packaged in the following ways: 1) Great Recalled by...
The Issue: Popcorn may contain foreign material: tempered glass between 3 mm and 7 mm...
Recommended Action: Do not consume. Return to store for a refund or discard.