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 3718137200 of 55,415 recalls

FoodApril 19, 2016· CSM Bakery Products NA

Recalled Item: 1.25 oz. TranSmart Recalled by CSM Bakery Products NA Due to Undeclared Allergen

The Issue: Undeclared allergen; Peanut protein.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 19, 2016· Elekta, Inc.

Recalled Item: Radionuclide Radiation Therapy System Product The product is a teletherapy...

The Issue: The latches of the frame adapter can be locked even if the locating pins of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2016· Synthes (USA) Products LLC

Recalled Item: 3.2 mm Three-fluted drill bit Recalled by Synthes (USA) Products LLC Due to...

The Issue: The sterile packaging may be compromised. A protective cap is to be secured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2016· Synthes (USA) Products LLC

Recalled Item: 3.2 mm three-fluted Radiolucent Drill Bit/Needle Point/145 mm Sterile...

The Issue: The sterile packaging may be compromised. A protective cap is to be secured...

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

Class II — Potential Health HazardOngoing
DrugApril 18, 2016· VistaPharm, Inc.

Recalled Item: Oxycodone Hydrochloride Oral Solution Recalled by VistaPharm, Inc. Due to...

The Issue: Defective Container: Excess lidding material accumulation between the seal...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 15, 2016· Zimmer Trabecular Metal Technology, Inc.

Recalled Item: POROUS PATELLA 32MM X 10MM - 00587806532 POROUS PATELLA 35MM Recalled by...

The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· 2k Innovations Inc.

Recalled Item: Volt Resistance Heated Slipper Gray (All sizes) Deep penetrating heat...

The Issue: During an FDA inspection it was found that the firm claims unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· 2k Innovations Inc.

Recalled Item: Volt Resistance Heated Slipper (All sizes) Deep penetrating heat garment...

The Issue: During an FDA inspection it was found that the firm claims unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· 2k Innovations Inc.

Recalled Item: Volt Resistance Heated Slipper Black (All sizes) Deep penetrating heat...

The Issue: During an FDA inspection it was found that the firm claims unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· 2k Innovations Inc.

Recalled Item: Volt Resistance Heated Socks (All sizes) Deep penetrating heat garment...

The Issue: During an FDA inspection it was found that the firm claims unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· 2k Innovations Inc.

Recalled Item: Volt Resistance Heated Therapy Shoulder Wrap Deep penetrating heat garment...

The Issue: During an FDA inspection it was found that the firm claims unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· 2k Innovations Inc.

Recalled Item: Volt Resistance Heated Elbow Garment Deep penetrating heat garment and wraps...

The Issue: During an FDA inspection it was found that the firm claims unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Biomerieux France Chemin De L'Or

Recalled Item: VIDAS NT-pro-BNP Product Usage: VIDAS¿ NTproBNP (PBNP) is an automated...

The Issue: Due to a packaging error; The kit does not contain the correct number of C1...

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

Class III — Low RiskOngoing
Medical DeviceApril 15, 2016· Zimmer Trabecular Metal Technology, Inc.

Recalled Item: 00720504022 ACETAB.CUPW/SH Recalled by Zimmer Trabecular Metal Technology,...

The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Zimmer Trabecular Metal Technology, Inc.

Recalled Item: REV. SHELL LINER 0D 28X48 00700504828 REV. SHELL LINER 10D Recalled by...

The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Zimmer Trabecular Metal Technology, Inc.

Recalled Item: TM CR TIB SZ 3 C-H Recalled by Zimmer Trabecular Metal Technology, Inc. Due...

The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· 2k Innovations Inc.

Recalled Item: Volt Resistance Heated Neck Garment Deep penetrating heat garment and wraps...

The Issue: During an FDA inspection it was found that the firm claims unapproved...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Zimmer Trabecular Metal Technology, Inc.

Recalled Item: TM MONO TIB STR GRN SZ 5 - 00588606510 TM Recalled by Zimmer Trabecular...

The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· Zimmer Trabecular Metal Technology, Inc.

Recalled Item: TM LPS TIB SZ 3 C/D Recalled by Zimmer Trabecular Metal Technology, Inc. Due...

The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2016· 2k Innovations Inc.

Recalled Item: Volt Resistance Heated Lower Back Garment Deep penetrating heat garment...

The Issue: During an FDA inspection it was found that the firm claims unapproved...

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

Class II — Potential Health HazardOngoing