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. 1,888 recalls have been distributed to Ohio in the last 12 months.
Showing 31461–31480 of 55,415 recalls
Recalled Item: Accu2i pMTA Applicator Recalled by Angiodynamics, Inc. Due to The firm is...
The Issue: The firm is recalling product that has the potential to not function during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RED SEXP DSTL FEM 19CM RT ASSY Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CER OPTION TYPE 1 TPR SLEVE -6 Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Natural Nail System Tear Drop Guide Wire 3.0 mm Diameter Recalled by...
The Issue: The design verification for the previous packaging configuration G928 does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CER BIOLOXD OPTION HD 32MM Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Possibility that the patient label inside the product box was incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu2i pMTA Applicator Recalled by Angiodynamics, Inc. Due to The firm is...
The Issue: The firm is recalling product that has the potential to not function during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M/DN Intramedullary Fixation Humeral Guide Wire - Bullet Tip 2.4 Recalled by...
The Issue: The design verification for the previous packaging configuration G928 does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M/DN Intramedullary Fixation Humeral Guide Wire - Smooth 2.4 mm Recalled by...
The Issue: The design verification for the previous packaging configuration G928 does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity 7 Recalled by St. Jude Medical, Inc. Due to The firm discovered a...
The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim 7 Elite Recalled by St. Jude Medical, Inc. Due to The firm...
The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD DISPOZ-A-BAG Leg Bag with Flip-Flo Valve with Drain Extension Recalled...
The Issue: Customer complaint of a cut in the side of the leg bag, indicating a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity 5 Recalled by St. Jude Medical, Inc. Due to The firm discovered a...
The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity 7 Recalled by St. Jude Medical, Inc. Due to The firm discovered a...
The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim 5 Elite Recalled by St. Jude Medical, Inc. Due to The firm...
The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: St. Jude Medical. Agilis NxT Steerable Introducer: B1-Directional Recalled...
The Issue: Inadequate seal due to lack of adhesive glue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity 5 Recalled by St. Jude Medical, Inc. Due to The firm discovered a...
The Issue: The firm discovered a risk of loss of Neuromodulation therapy due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G & W Clobetasol Propionate Ointment 0.05% Recalled by G & W Laboratories,...
The Issue: Failed impurities/degradation specifications: This product is being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Southern Grove Cashew Halves & Pieces with Sea Salt Recalled by Star Snacks...
The Issue: The firm received notification from a consumer finding a glass fragment in...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Salinity sea salt Saltwell Recalled by AB HANSON AND MOHRING Due to Foreign...
The Issue: pieces of foreign material in product
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Option 2 Recalled by L. Perrigo Company Due to Defective Container: Carton...
The Issue: Defective Container: Carton is missing the tablet blister strip and tablet.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.