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 3750137520 of 55,415 recalls

Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Cotton Balls-Strung 1/2" : 30-02 Product Usage: Recalled...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Cotton Balls-Strung 3/4" : 30-03 Product Usage: Recalled...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Americot Blue 1/2" x 1.5" : 20-06S Recalled by American...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· Siemens Medical Solutions USA, Inc.

Recalled Item: E.cam or Symbia systems that use foresight detectors - Product Recalled by...

The Issue: E. CAM and Symbia system with foresight detectors performing gated or...

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

Class II — Potential Health HazardOngoing
DrugMarch 30, 2016· Dr. Reddy's Laboratories, Inc.

Recalled Item: Ondansetron Tablets USP Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications; 12 month stability time point

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 30, 2016· Teleflex Medical

Recalled Item: Pleur-evac Chest Drainage System Recalled by Teleflex Medical Due to The...

The Issue: The label on the Tyvek bag is missing. This is used by customers to identify...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur CP Immunoassay System Recalled by Siemens Healthcare...

The Issue: The firm identified an issue in sample processing when using EZee-Nest...

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

Class III — Low RiskOngoing
Medical DeviceMarch 29, 2016· ev3, Inc.

Recalled Item: ev3 Recalled by ev3, Inc. Due to Mislabeling

The Issue: Medtronic is conducting a voluntary Urgent Medical Device Recall of two lots...

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

Class II — Potential Health HazardOngoing
FoodMarch 29, 2016· Lee Seed Co Inc

Recalled Item: Yogurt Super Soynuts packaged in 16 oz. plastic bags and Recalled by Lee...

The Issue: Product contains undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 28, 2016· R.W. Bakers Co. Inc.

Recalled Item: Assorted Dinner Rolls Recalled by R.W. Bakers Co. Inc. Due to Undeclared Peanuts

The Issue: R.W. Bakers Co. of Muskegon, MI, is recalling its 8 ct. packages of "Meijer...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 28, 2016· R.W. Bakers Co. Inc.

Recalled Item: Meijer Plain Knot Rolls Recalled by R.W. Bakers Co. Inc. Due to Undeclared...

The Issue: R.W. Bakers Co. of Muskegon, MI, is recalling its 8 ct. packages of "Meijer...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 28, 2016· Philips Ultrasound, Inc.

Recalled Item: EPIQ DIAGNOSTIC ULTRASOUND SYSTEM Recalled by Philips Ultrasound, Inc. Due...

The Issue: The fasteners securing the control panel assembly to the base of the Philips...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Becton Dickinson & Co.

Recalled Item: Trypticase TM Soy Agar with 5% Sheep Blood (TSA IITM) Recalled by Becton...

The Issue: Trypticase TM Soy Agar with 5% Sheep Blood (TSA IITM) // MacConkey II Agar...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Stryker Endoscopy

Recalled Item: PneumoSure XL High Flow Insufflator and PneumoSure High Flow Insufflator...

The Issue: When operating the device in high flow mode (40L/min, 15 mmHg) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Boston Scientific Corporation

Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...

The Issue: Boston Scientific is voluntarily implementing a Medical Device Recall of one...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Eye Station Import Utility (ESIU) when used with Merge Recalled by...

The Issue: Eye Station images were not importing properly and were imported under...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Merge Healthcare, Inc.

Recalled Item: Merge PACS software. Product Usage: Merge PACS (Picture Archiving...

The Issue: The software did not show unviewed images when the last view was skipped....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Hemo software. Merge Hemo monitors Recalled by Merge Healthcare, Inc....

The Issue: There is a potential connection issue when powering up the Merge Hemo Record...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Cardio software. Merge Cardio is a system intended to Recalled by...

The Issue: If images are sent without an order in the system, they will be matched with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Merge Healthcare, Inc.

Recalled Item: Merge PACS software. Merge PACS (Picture Archiving Communication System) is...

The Issue: Cut lines on the image may present horizontally rather than vertically.

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

Class II — Potential Health HazardOngoing