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 3692136940 of 55,415 recalls

Medical DeviceMay 2, 2016· Synthes (USA) Products LLC

Recalled Item: 1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 24 mm - Sterile...

The Issue: Labeling errors. The outer packge label expiration date may exceed the...

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

Class II — Potential Health HazardOngoing
DrugMay 2, 2016· Sandoz, Inc

Recalled Item: Dicloxacillin Sodium Capsules Recalled by Sandoz, Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications:Out of specification result for...

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

Class III — Low RiskOngoing
Refund
DrugMay 2, 2016· Sandoz, Inc

Recalled Item: Dicloxacillin Sodium Capsules USP Recalled by Sandoz, Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications:Out of specification result for...

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

Class III — Low RiskOngoing
Refund
DrugApril 29, 2016· Making It a Lifestyle

Recalled Item: BLACK LABEL X capsules Recalled by Making It a Lifestyle Due to Undeclared...

The Issue: Marketed without an approved NDA/ANDA - presence of undeclared sildenafil.

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 29, 2016· Making It a Lifestyle

Recalled Item: 3rd DEGREE capsules Recalled by Making It a Lifestyle Due to Undeclared...

The Issue: Marketed without an approved NDA/ANDA - presence of undeclared sibutramine.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 29, 2016· Making It a Lifestyle

Recalled Item: BLACK GOLD X ADVANCED capsules Recalled by Making It a Lifestyle Due to...

The Issue: Marketed without an approved NDA/ANDA - presence of undeclared sibutramine.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 29, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity CT Model No. 728326 Recalled by Philips Medical Systems...

The Issue: Software issues in v4.1.3/4.1.4/4.1.5 in the Philips Ingenuity CT products...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT SP Model No. 728311 Recalled by Philips Medical Systems...

The Issue: Software issues found in v4.1 .3/4.1.5 in the Philips Brilliance iCT/ iCT SP...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core128 Model No. 728323 Recalled by Philips Medical Systems...

The Issue: Software issues in v4.1.3/4.1.4/4.1.5 in the Philips Ingenuity CT products...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: Software issues in versions v4.1 .3/4.1.5 in the Philips Brilliance iCT) iCT...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 CT Model 728231 Recalled by Philips Medical Systems...

The Issue: Software issues found in software versions v4.1.3/4.1.4/4.1.5 in the Philips...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core Model No. 728321 Recalled by Philips Medical Systems...

The Issue: Software issues in software versions v4.1.3/4.1.4/4.1.5 in the Philips...

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

Class II — Potential Health HazardOngoing
FoodApril 29, 2016· O'Steen Meat Specialties, Inc.

Recalled Item: Code 2013 Spicy Mac & Cheese Bites Breaded Macaroni & Recalled by O'Steen...

The Issue: Potential plastic inclusion.

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 28, 2016· Giant Eagle, Inc.

Recalled Item: Pecan Tassie - 6 Pack PLU# 77997 Net Wt. 5 OZ. Sell By (dates up to) May 03...

The Issue: Giant Eagle discovered that the scale label fails to declare the milk...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 28, 2016· Giant Eagle, Inc.

Recalled Item: Walnut Delights 6 Pack Net Weight: 9 oz. PLU #69690 Recalled by Giant Eagle,...

The Issue: Giant Eagle discovered that the scale label fails to declare the milk...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 28, 2016· Giant Eagle, Inc.

Recalled Item: Small Cookie Tray Recalled by Giant Eagle, Inc. Due to Giant Eagle...

The Issue: Giant Eagle discovered that the ingredient statement for Pecan Tassies fails...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 28, 2016· Excelsior Medical Corp

Recalled Item: Excelsior Disposable Syringe Heparin Lock Flush Recalled by Excelsior...

The Issue: Certain lots of Heparin Lock Flush, USP Syringes (5 ml Fill in 10 ml...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Maestro Air Motor Pneumatic cranial drill motor. The Maestro Air Recalled by...

The Issue: Due to the buildup of grease within the hose and motor, the product may...

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

Class II — Potential Health HazardOngoing
DrugApril 28, 2016· Pfizer Inc.

Recalled Item: Zoloft (sertraline HCl) tablets Recalled by Pfizer Inc. Due to Failed...

The Issue: Failed Tablet/Capsule Specifications: thick tablets exceeding specifications...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 28, 2016· Lymol Medical

Recalled Item: Sclerosol Intrapleural Aerosol (sterile talc powder) Recalled by Lymol...

The Issue: Defective Delivery System: Defective stem valve causes leakage of the...

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

Class II — Potential Health HazardOngoing
Refund