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 27441–27460 of 55,415 recalls
Recalled Item: SPARKLING GRAPEFRUIT JUICE DRINK Recalled by Gourmet International Inc. Due...
The Issue: Gourmet International Inc. is voluntarily recalling LItaly Sparkling Juice...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: SPARKLING SOUR CHERRY JUICE DRINK Recalled by Gourmet International Inc. Due...
The Issue: Gourmet International Inc. is voluntarily recalling LItaly Sparkling Juice...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: SPARKLING LEMON JUICE DRINK Recalled by Gourmet International Inc. Due to...
The Issue: Gourmet International Inc. is voluntarily recalling LItaly Sparkling Juice...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: SPARKLING LIME JUICE DRINK Recalled by Gourmet International Inc. Due to...
The Issue: Gourmet International Inc. is voluntarily recalling LItaly Sparkling Juice...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DORO LUCENT Transitional Member Recalled by Pro-Med Instruments Gmbh Due to...
The Issue: The combination of two different design revisions of DORO LUCENT Base Unit,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DORO LUCENT Base Unit Recalled by Pro-Med Instruments Gmbh Due to The...
The Issue: The combination of two different design revisions of DORO LUCENT Base Unit,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DORO LUCENT Locking Transitional Member Recalled by Pro-Med Instruments Gmbh...
The Issue: The combination of two different design revisions of DORO LUCENT Base Unit,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monsel's Solution (Ferric Subsulfate) Recalled by Medgyn Products, Inc. Due...
The Issue: CGMP Deviations: The manufacturer of this product recalled because they were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PINK LEMONADE COOKIES Byrd's FAMOUS COOKIES Recalled by Byrd Cookie Co Due...
The Issue: Red 40 & Red 3 were not listed in the ingredients statement
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PLUS 30 PRIORITY PACK Accessory Kit Product Usage: Is recommended Recalled...
The Issue: Incorrect expiration being entered for one lot.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL800 analyzer Recalled by Radiometer America Inc Due to The analyzer...
The Issue: The analyzer software may cause a mis-match of patient demographics and test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zenlens Toric-Gas Permeable Contact lenses for Daily Wear in a Recalled by...
The Issue: Vials labeled for the prescriptions contained incorrect lenses
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zen RC Toric-Gas permeable contact lenses for Daily Wear in Recalled by...
The Issue: Vials labeled for the prescriptions contained incorrect lenses
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AbViser AutoValve IAP (intra- abdominal pressure) Monitoring Device Recalled...
The Issue: Bubble Leak Testing on AbViser AutoValve IAP Monitoring Devices without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piperacillin and Tazobactam for Injection USP 3.375 grams per vial Recalled...
The Issue: Presence of Particulate Matter: identified as glass and silicone material
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Product: ABL800 FLEX with Crea. The ABL800 with Crea is Recalled by...
The Issue: From three incidents in Denmark and Sweden, comparison studies on patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Powder Free Vinyl Exam Gloves Recalled by Cypress Medical Products LLC Due...
The Issue: The firm is recalling one lot of McKesson Powder Free Vinyl Exam Gloves...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTOVi Tracker/Scanner Recalled by Hudson Scientific LLC Due to The device...
The Issue: The device and its accessories may not have been manufactured according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Waterpik Sonic-Fusion Professional Recalled by Water Pik, Inc. Due to...
The Issue: Charging base may overheat with localized melting and sparking, possibly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neostigmine Methylsulfate Injection Solution Recalled by Fagron Compounding...
The Issue: Labeling: Label Error on Declared Strength: syringes of Neostigmine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.