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. 2,128 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
2,128 in last 12 months

Showing 56815700 of 55,415 recalls

Medical DeviceJune 7, 2024· Integra LifeSciences Corp.

Recalled Item: AURORA Surgiscope System. Sterile Recalled by Integra LifeSciences Corp. Due...

The Issue: Potential sheath damage that could lead to tissue damage and/or track...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2024· Philips North America Llc

Recalled Item: SENSE XL TORSO COIL 1.5T Mk2. 16-element receive only coil Recalled by...

The Issue: Potential for coils to heat up and harm patients (burn).

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJune 5, 2024· Philips North America Llc

Recalled Item: SENSE XL TORSO COIL 3.0T. 16-element receive only coil for Recalled by...

The Issue: Potential for coils to heat up and harm patients (burn).

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJune 5, 2024· Philips North America Llc

Recalled Item: SENSE XL TORSO COIL 1.5T. 16-element receive only coil for Recalled by...

The Issue: Potential for coils to heat up and harm patients (burn).

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJune 5, 2024· Beckman Coulter Mishima K.K.

Recalled Item: DxC 500 AU Clinical Chemistry Analyzer Recalled by Beckman Coulter Mishima...

The Issue: There are two software bug issues with the analyzer. Issue 1: When a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJune 5, 2024· Homeocare Laboratories, Inc.

Recalled Item: STELLALIFE VEGA Oral Care Recalled by Homeocare Laboratories, Inc. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: multiple Bacillus species...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugJune 5, 2024· Homeocare Laboratories, Inc.

Recalled Item: STELLALIFE ADVANCED FORMULA Peppermint Recalled by Homeocare Laboratories,...

The Issue: Microbial Contamination of Non-Sterile Products: presence of Terribacillus...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 4, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: Eszopiclone Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Related Substances

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugJune 4, 2024· Teva Pharmaceuticals USA, Inc

Recalled Item: Amoxicillin and Clavulanate Potassium Tablets USP Recalled by Teva...

The Issue: Subpotent Drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 4, 2024· Zyno Medical LLC

Recalled Item: Zyno Medical Z800 Recalled by Zyno Medical LLC Due to Zyno Medical has found...

The Issue: Zyno Medical has found that certain Z800, Z800F, Z800W, and Z800WF pumps...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2024· Beckman Coulter, Inc.

Recalled Item: Dxl 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...

The Issue: The analyzers were built with nonconforming USB cables made with brass...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· Stryker Corporation

Recalled Item: The Non-Sterile Flyte hood covers the user s head and Recalled by Stryker...

The Issue: Expired Products distributed to customers

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· Microtek Medical Inc.

Recalled Item: Vial Decanter Recalled by Microtek Medical Inc. Due to During sterile...

The Issue: During sterile barrier testing performed on the decanter product line, the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: 190828: 2008K@HOME HEMODIALYSIS SYSTEM - Blood Pump Rotor spare part...

The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: 191014: 2008K@HOME HD SYSTEM W/BIBAG (CANADA) - Blood Pump Rotor spare part...

The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· Qiagen Sciences LLC

Recalled Item: QIAcube Connect MDx - IVD Instrument designed to perform automated Recalled...

The Issue: Heater shaker module does not perform heating if the temperature is set...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: RTL190828: 2008K@HOME HEMODIALYSIS SYSTEM - Blood Pump Rotor spare part...

The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: RTL190904: 2008K@HOME HEMODIALYSIS SYSTEM W/ BIBAG - Blood Pump Rotor spare...

The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· Microtek Medical Inc.

Recalled Item: Bottle Decanter Recalled by Microtek Medical Inc. Due to During sterile...

The Issue: During sterile barrier testing performed on the decanter product line, the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· ASPEN SURGICAL

Recalled Item: Endoscopic Kittner Blunt Dissecting Instrument Recalled by ASPEN SURGICAL...

The Issue: The affected products may have been packaged with a defect in the sterile...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing