Product Recalls in Indiana

Product recalls affecting Indiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Indiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,577 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,577 in last 12 months

Showing 2168121700 of 53,528 recalls

Medical DeviceSeptember 12, 2019· Merit Medical Systems, Inc.

Recalled Item: Custom Sheath Introducer Kit - Product Usage: intended Recalled by Merit...

The Issue: labeling error: Due to a manufacturing issue, product package was...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2019· Olympus Corporation of the Americas

Recalled Item: Berkeley Disposa-Filter used with Berkeley VC-10 Vacuum Curettage System -...

The Issue: Berkeley Disposa-Filter may possess an insufficient ultrasonic weld defect...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2019· Integra LifeSciences Corp.

Recalled Item: Cerelink ICP Monitor Recalled by Integra LifeSciences Corp. Due to There is...

The Issue: There is a potential for a progressive decline in observed ICP readings of...

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

Class II — Potential Health HazardOngoing
FoodSeptember 11, 2019· Lipari Foods Operating Company, LLC.

Recalled Item: Fresh Grab brand Ham & Cheese Recalled by Lipari Foods Operating Company,...

The Issue: FDA environmental sampling returned a positive test result for Listeria...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 11, 2019· Lipari Foods Operating Company, LLC.

Recalled Item: Premo and Fresh Grab brands Egg Salad Recalled by Lipari Foods Operating...

The Issue: FDA environmental sampling returned a positive test result for Listeria...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 11, 2019· Lipari Foods Operating Company, LLC.

Recalled Item: Fresh Grab brand Turkey No Cheese Recalled by Lipari Foods Operating...

The Issue: FDA environmental sampling returned a positive test result for Listeria...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 11, 2019· Lipari Foods Operating Company, LLC.

Recalled Item: Premo and Fresh Grab brands Chicken Salad Recalled by Lipari Foods Operating...

The Issue: FDA environmental sampling returned a positive test result for Listeria...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 11, 2019· Lipari Foods Operating Company, LLC.

Recalled Item: Premo and Fresh Grab brands Tuna Salad Recalled by Lipari Foods Operating...

The Issue: FDA environmental sampling returned a positive test result for Listeria...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 11, 2019· Lipari Foods Operating Company, LLC.

Recalled Item: Premo brand Bologna & Cheese Wedge Recalled by Lipari Foods Operating...

The Issue: FDA environmental sampling returned a positive test result for Listeria...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Ultrasound Transducer (M1356A) Recalled by Pacific Medical Group Inc. Due to...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Loop-Style Tocotransducer (Nautilus) 2264LAX Recalled by Pacific Medical...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Toco MP Transducer (M2734B) Recalled by Pacific Medical Group Inc. Due to...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Button-Style Ultrasound Transducer (Nautilus) Recalled by Pacific Medical...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Respironics California, LLC

Recalled Item: Respironics V60 Ventilator Recalled by Respironics California, LLC Due to...

The Issue: Ventilator touchscreen may become frozen and fail to respond to touch...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Toco M2734A Recalled by Pacific Medical Group Inc. Due to Fetal/maternal...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Loop-Style Ultrasound Transducer (Nautilus) Recalled by Pacific Medical...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Respironics California, LLC

Recalled Item: Respironics RP-Touch Screen Recalled by Respironics California, LLC Due to...

The Issue: Ventilator touchscreen may become frozen and fail to respond to touch...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: External Toco Transducer (M1355A) Recalled by Pacific Medical Group Inc. Due...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Respironics California, LLC

Recalled Item: Respironics RP-UI Assy Recalled by Respironics California, LLC Due to...

The Issue: Ventilator touchscreen may become frozen and fail to respond to touch...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Toco+ transducer with ECG/IUP capability (wired) Recalled by Pacific Medical...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing