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.
Showing 25341–25360 of 55,415 recalls
Recalled Item: QVC 3/8 oz bags for Christmas Recalled by Bauer's Candies, Inc. Due to Risk...
The Issue: Risk of Hepatitis A exposure.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sea Salt Bauer's Candies Modjeskas NET WT 8 oz bag Recalled by Bauer's...
The Issue: Risk of Hepatitis A exposure.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 1 lb salted combo modjeskas Recalled by Bauer's Candies, Inc. Due to Risk of...
The Issue: Risk of Hepatitis A exposure.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 8 oz assorted modjeska/chocolate modjeskas Recalled by Bauer's Candies, Inc....
The Issue: Risk of Hepatitis A exposure.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bulk assorted Recalled by Bauer's Candies, Inc. Due to Risk of Hepatitis A...
The Issue: Risk of Hepatitis A exposure.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bauer's Candies Caramels NET WT 4 oz (bag) & bulk Recalled by Bauer's...
The Issue: Risk of Hepatitis A exposure.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ROOT 23 CUCUMBER HABANERO SIMPLE SYRUP 375 ml Recalled by Root 23 LLC Due to...
The Issue: Non-compliance with process authority schedule; temperature at start of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Triton Sponge System (Software) Recalled by Stryker Instruments Div. of...
The Issue: Gauss Surgical is updating the Instructions for Use (IFU) for our Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition S Recalled by Philips Medical Systems Nederlands Due to...
The Issue: During automatic tabletop movement, pressing and holding the Stop Table...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C2 CryoBalloon Controller Recalled by PENTAX of America Inc Due to The...
The Issue: The Controller does not detect overpressure in the balloon during the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentax Medical C2 CryoBalloon Standard Focal Catheter Recalled by PENTAX of...
The Issue: Incorrect default dose and dose increments may be transmitted to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTotal CR Total Knee Replacement System Recalled by Conformis, Inc. Due to...
The Issue: The kits were prepared with incorrect patient ID labels and may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentax Medical C2 CryoBalloon Pear Focal Catheter Recalled by PENTAX of...
The Issue: Incorrect default dose and dose increments may be transmitted to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentax Medical C2 CryoBalloon Standard 90 degree Catheter Recalled by PENTAX...
The Issue: Incorrect default dose and dose increments may be transmitted to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST AIA-PACK Testosterone (TES) is designed for IN VITRO DIAGNOSTIC Recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST AIA-PACK Homocysteine (HCY) is designed for IN VITRO DIAGNOSTIC Recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-PACK Folate (FOL) is designed for IN VITRO DIAGNOSTIC USE Recalled by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Biograph Horizon PET/CT System Recalled by Siemens Medical Solutions...
The Issue: Improper design or specifications.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST AIA-PACK ACTH (ACTH: Adrenocorticotropic Hormone) is designed for IN...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-PACK B12 (Vitamin B12) is designed for IN VITRO DIAGNOSTIC Recalled by...
The Issue: Potential for fluorescein interference to cause inaccurately elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.