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. 2,593 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,593 in last 12 months

Showing 1912119140 of 53,528 recalls

Medical DeviceJune 17, 2020· Resource Optimization & Innovation LLC

Recalled Item: regard Migrating Indicator Recalled by Resource Optimization & Innovation...

The Issue: The firm received reports from customer that the Regard Migrating Indicator...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2020· Wellspect HealthCare (Division of DENTSPLY IH AB)

Recalled Item: LoFric Origo Recalled by Wellspect HealthCare (Division of DENTSPLY IH AB)...

The Issue: Wellspect Healthcare is voluntarily recalling certain LoFric¿ Origo"...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2020· Wellspect HealthCare (Division of DENTSPLY IH AB)

Recalled Item: LoFric Origo Recalled by Wellspect HealthCare (Division of DENTSPLY IH AB)...

The Issue: Wellspect Healthcare is voluntarily recalling certain LoFric¿ Origo"...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2020· Wellspect HealthCare (Division of DENTSPLY IH AB)

Recalled Item: LoFric Origo Recalled by Wellspect HealthCare (Division of DENTSPLY IH AB)...

The Issue: Wellspect Healthcare is voluntarily recalling certain LoFric¿ Origo"...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2020· FHC, Inc.

Recalled Item: FHC Guideline 4000 5.0 GL5 Main Processing Unit - Product Recalled by FHC,...

The Issue: An electrical sub-circuit was not properly connected. Its purpose is to...

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

Class II — Potential Health HazardOngoing
DrugJune 16, 2020· Glaxosmithkline Consumer Healthcare Holdings

Recalled Item: Childrens Dimetapp Cold & Cough Recalled by Glaxosmithkline Consumer...

The Issue: Defective Delivery System: the dosing cups are missing graduations...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 16, 2020· Glaxosmithkline Consumer Healthcare Holdings

Recalled Item: Childrens Robitussin Honey Cough and Chest Congestion DM Recalled by...

The Issue: Defective Delivery System: the dosing cups are missing graduations...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to Infusion...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: BodyGuard Microset With Female Luer Recalled by CME America, LLC Due to...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to Infusion...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: BodyGuard BodySet Recalled by CME America, LLC Due to Infusion...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to Infusion...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: CMExpress Microbore Sets Recalled by CME America, LLC Due to Infusion...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: BodyGuard Microset w/ 0.2 mic filter and lower y-site with female luer...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: BodyGuard set with Female Luer Recalled by CME America, LLC Due to Infusion...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to Infusion...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: BodyGuard Microset with Filter Recalled by CME America, LLC Due to Infusion...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: BodyGuard Microset with Filter and Manual Priming Valve Recalled by CME...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: Standard BodySet with Needleless Connectors Recalled by CME America, LLC Due...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to Infusion...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing