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.

55,415 total recalls
2,542 in last 12 months

Showing 3738137400 of 55,415 recalls

Medical DeviceApril 1, 2016· Biomet, Inc.

Recalled Item: Various trauma and sports medicine instruments and implants. guide Recalled...

The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· Biomet, Inc.

Recalled Item: Various trauma and sports medicine instruments and implants. Pin Recalled by...

The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· Biomet, Inc.

Recalled Item: Various trauma and sports medicine instruments and implants. Appliance...

The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· Biomet, Inc.

Recalled Item: Various trauma and sports medicine instruments and implants. Rod Recalled by...

The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· Biomet, Inc.

Recalled Item: Various trauma and sports medicine instruments and implants. Spinal...

The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· Applied Medical Resources Corp

Recalled Item: Direct Drive Clip Applier CA090 Recalled by Applied Medical Resources Corp...

The Issue: Increased customer complaints indicating inconsistent clip application; may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· Biomet, Inc.

Recalled Item: Various trauma and sports medicine instruments and implants. Screw Recalled...

The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core 128-Computed Tomography X-ray system Product Usage: The...

The Issue: Philips Healthcare received reports from the field that certain Ingenuity...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· Biomet, Inc.

Recalled Item: Various trauma and sports medicine instruments and implants. Arthroscope....

The Issue: Insufficient seal strength on sterile barrier packaging. The seal could be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: Philips Healthcare received reports from the field that certain Brilliance...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Smart CR Digital Computed Radiography System Recalled by Fujifilm Medical...

The Issue: Reports of failure of the device's power supply.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2016· B Braun Medical Inc

Recalled Item: Dialog+ Hemodialysis machines: Conductivity Sensor (BIC) Item 3456103A The...

The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2016· B Braun Medical Inc

Recalled Item: Dialog+ Hemodialysis machines: Dialog A + 1 Blood Pump 120V Recalled by B...

The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2016· B Braun Medical Inc

Recalled Item: Dialog+ Hemodialysis machines: Dialog A + HE/BIC Product Code 710200L...

The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2016· B Braun Medical Inc

Recalled Item: Dialog+ Hemodialysis machines: Conductivity Sensor (BIC) Item # 3456102A The...

The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2016· B Braun Medical Inc

Recalled Item: Dialog+ Hemodialysis machines: Dialog + 120 V DF+Adimea+WAN-BSL Product Code...

The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2016· B Braun Medical Inc

Recalled Item: Dialog+ Hemodialysis machines: Dialog + 120 V DF+Adimea+WAN-BSL-BIC Product...

The Issue: Potential leakage of conductivity sensors of the Dialog Dialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Force Recalled by Siemens Medical Solutions USA, Inc Due to The...

The Issue: The Neonate Head protocol with the pediatric kernel Hp38 could result in...

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

Class II — Potential Health HazardOngoing
FoodApril 1, 2016· Roland Foods, LLC.

Recalled Item: Roland (R) Fire Roasted Red Pepper Strips Recalled by Roland Foods, LLC. Due...

The Issue: Possible presence of glass fragments in the product lots.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodApril 1, 2016· Sugarfina, LLC

Recalled Item: Sugarfina Chocolate Malt Balls Code 840278113565 SKU K1159 Recalled by...

The Issue: undeclared peanuts

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund