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. 2,462 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,462 in last 12 months

Showing 22612280 of 29,228 recalls

Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 8H LT: Anatomic Lateral Fibula Plate...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX - ANATOMIC LAT FIB PLATE 4H LT: Anatomic Lateral Fibula Plate...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX -ANATOMIC LAT FIB PLATE 4H RT: Anatomic Lateral Fibula Plate...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX- MEDIAL TIBIA PLATE 6H RT-Medial Tibia Plate Recalled by Tyber...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX- ANATOMIC LAT FIB PLATE 10H RT- Anatomic Lateral Fibula Plate...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX- MEDIAL TIBIA PLATE 16H LT-Medial Tibia Plate Recalled by Tyber...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX -ANATOMIC LAT FIB PLATE 6H LT- Anatomic Lateral Fibula Plate...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2025· Tyber Medical

Recalled Item: A.L.P.S. mvX-P: ANATOMIC LAT FIB PLATE 12H LT- Anatomic Lateral Fibula Plate...

The Issue: Complaints of the locking screw passing through the locking hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2025· Microbiologics Inc

Recalled Item: Microbiologics Multi-Strain Human Papillomavirus (HPV) Verification Panel...

The Issue: Internal quality control procedures were not followed correctly for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2025· Microbiologics Inc

Recalled Item: Microbiologics Multi-Strain Human Papillomavirus (HPV) Control Panel...

The Issue: Internal quality control procedures were not followed correctly for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2025· KCI USA, INC.

Recalled Item: 3M V.A.C. VIA Negative Pressure Wound Therapy System /US Recalled by KCI...

The Issue: Due to increase in complaints related to leak alarms

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2025· KCI USA, INC.

Recalled Item: 3M Prevena Plus 125 Therapy Unit and System Kits by KCI USA, INC. Due to Due...

The Issue: Due to increase in complaints related to leak alarms

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2025· Zhejiang Luyao Electronics Technology Co., Ltd.

Recalled Item: Brand Name: HOMEDICS Product Name: Air Compression Leg Massager...

The Issue: Regulatory documentation error and misleading color packaging claim.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: Brand Name: RayStation -Intended as a Radiation Therapy Treatment Planning...

The Issue: Inconsistency in the use of Density uncertainty in the RayStation functions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: Brand Name: RayStation- Intended as a Radiation Therapy Treatment Planning...

The Issue: Inconsistency in the use of Density uncertainty in the RayStation functions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: Brand Name: RayStation- Intended as a Radiation Therapy Treatment Planning...

The Issue: Inconsistency in the use of Density uncertainty in the RayStation functions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: Brand Name: RayStation- Intended as a Radiation Therapy Treatment Planning...

The Issue: Inconsistency in the use of Density uncertainty in the RayStation functions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: Brand Name: RayStation -Intended as a Radiation Therapy Treatment Planning...

The Issue: Inconsistency in the use of Density uncertainty in the RayStation functions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: Brand Name: RayStation Intended as a Radiation Therapy Treatment Planning...

The Issue: Inconsistency in the use of Density uncertainty in the RayStation functions...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2025· Scientia Vascular, Inc.

Recalled Item: Plato 17 Microcatheter To assist in delivery of Recalled by Scientia...

The Issue: Due to manufacturing non-conformance that resulted in channels in the seal...

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

Class II — Potential Health HazardOngoing