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. 2,768 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,768 in last 12 months

Showing 18411860 of 29,228 recalls

Medical DeviceMarch 27, 2025· Galt Medical Corporation

Recalled Item: GALT Centeze Catheter DRC-002-06 The Centeze is intended Recalled by Galt...

The Issue: Due to a potential open seal in the sterile barrier packaging .

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2025· IHB OPERATIONS B.V.

Recalled Item: Skytron Freedom 4FXS-60 Heavy Duty Monitor Mount Recalled by IHB OPERATIONS...

The Issue: The mounting hardware that is supplied with the 4FXS-60 monitor bracket does...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2025· Conformis Inc.

Recalled Item: restor3d Cordera Hip System. ACETABULAR LINER GRP C 36MM LIP. Recalled by...

The Issue: The hip cup liner that was packaged with the incorrect labeling....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Intera 1.5T Explorer/Nova Dual Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Intera 1.5T Master/Nova Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: SmartPath to dStream for 3.0T Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: SmartPath to dStream for 1.5T Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Intera 1.0T Omni/Stellar Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Enterprise 1.5T Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Intera 1.5T Omni/Stellar Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Intera 0.5T Standard Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Intera 3.0T Quasar Dual Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Intera 1.5T Power/Pulsar Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Intera 1.5T R11 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Intera 1.5T Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to The...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Intera 1.0T Power/Pulsar Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Intera CV Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to The...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Meridian Bioscience ImmunoCard STAT! Crypto/Giardia Test Kits Recalled by...

The Issue: A single lot of the ImmunoCard STAT! Crypto/Giardia Test Kit was...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· Boston Scientific Corporation

Recalled Item: IceSeed 1.5 CX S NEEDLE OUS Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has identified that IceSeedTM CX needles manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2025· Boston Scientific Corporation

Recalled Item: IceSeed 1.5 CX NEEDLE OUS Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has identified that IceSeedTM CX needles manufactured...

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

Class II — Potential Health HazardOngoing