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. 2,580 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
2,580 in last 12 months

Showing 2862128640 of 55,415 recalls

Medical DeviceMarch 7, 2018· Ethicon, Inc.

Recalled Item: Evicel Accessory Device - 45 cm Flexible Tip (SET OF 3) Recalled by Ethicon,...

The Issue: Products labeled for distribution outside the United States may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Edwards Lifesciences Thin-Flex Single Stage Venous Drainage Cannula Recalled...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Edwards Lifesciences Femoral Venous Cannula Recalled by SPS Sterilization,...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Edwards Lifesciences EZ Glide Aortic Cannula Recalled by SPS Sterilization,...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Edwards Lifesciences Optisite Arterial Perfusion Cannula Recalled by SPS...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Edwards Lifesciences Femoral Venous Cannula Recalled by SPS Sterilization,...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Boston Scientific Wallstent RP Endoprosthesis Tracheobronchial...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Boston Scientific Wallstent Endoprosthesis Tracheobronchial Self-Expanding...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Edwards Lifesciences Avid Dual Stage Venous Drainage Cannula Recalled by SPS...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Boston Scientific Wallstent Endoprosthesis Tracheobronchial Self-Expanding...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Edwards Lifesciences Thin-Flex Single Stage Venous Drainage Cannula Recalled...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Boston Scientific Wallstent RP Endoprosthesis Tracheobronchial Transhepatic...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Edwards Lifesciences Aortic Perfusion Cannula Recalled by SPS Sterilization,...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· Intuitive Surgical, Inc.

Recalled Item: da Vinci X Surgical System Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Specific da Vinci X Surgical Systems (IS4200) were shipped with defective...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Boston Scientific Wallstent Enteral Endoprosthesis Colonic/Duodenal Stent...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Boston Scientific Wallstent Endoprosthesis Tracheobronchial Transhepatic...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Vascular Solutions Venture Rx Catheter Recalled by SPS Sterilization, Inc...

The Issue: The expiration date on the device labeling exceeds its actual validated...

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

Class II — Potential Health HazardOngoing
FoodMarch 6, 2018· Piggie Park Enterprises Inc

Recalled Item: Maurice's Honey Southern Gold BBQ Sauce Recalled by Piggie Park Enterprises...

The Issue: Undeclared soy and wheat ingredients

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 5, 2018· Kodiak Cakes, LLC

Recalled Item: Kodiak Cakes Recalled by Kodiak Cakes, LLC Due to The frozen waffle product...

The Issue: The frozen waffle product contains whey but fails to declare the major food...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 5, 2018· Tosoh Bioscience Inc

Recalled Item: ST-AIA PACK hsE2 Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...

The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...

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

Class II — Potential Health HazardOngoing