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 19011920 of 29,228 recalls

Medical DeviceMarch 19, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: It was identified that the Medline Sterile Water and Medline Sterile 0.9%...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: It was identified that the Medline Sterile Water and Medline Sterile 0.9%...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2025· Siemens Healthcare Diagnostics Inc

Recalled Item: epoc BGEM Crea Test Card (25 pk) for the epoc Blood Analysis System Recalled...

The Issue: The occurrence of discrepant high pH results in samples introduced with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2025· Avanos Medical, Inc.

Recalled Item: Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog...

The Issue: Lack of sterility assurance for closed suction catheter systems

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 19, 2025· Avanos Medical, Inc.

Recalled Item: Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog...

The Issue: Lack of sterility assurance for closed suction catheter systems

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 19, 2025· Avanos Medical, Inc.

Recalled Item: Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog...

The Issue: Lack of sterility assurance for closed suction catheter systems

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 19, 2025· Avanos Medical, Inc.

Recalled Item: Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog...

The Issue: Lack of sterility assurance for closed suction catheter systems

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 19, 2025· Avanos Medical, Inc.

Recalled Item: Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog...

The Issue: Lack of sterility assurance for closed suction catheter systems

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 19, 2025· Avanos Medical, Inc.

Recalled Item: Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog...

The Issue: Lack of sterility assurance for closed suction catheter systems

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 19, 2025· Avanos Medical, Inc.

Recalled Item: Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog...

The Issue: Lack of sterility assurance for closed suction catheter systems

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 19, 2025· Avanos Medical, Inc.

Recalled Item: Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog...

The Issue: Lack of sterility assurance for closed suction catheter systems

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 18, 2025· Smith & Nephew, Inc.

Recalled Item: META-TAN LAG/COMPRESSION SCREW KIT 90MM/85MM Recalled by Smith & Nephew,...

The Issue: Integrated Lag/Compression Screw Kit has a compression screw with hexagon...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2025· Abbott Laboratories

Recalled Item: Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number:...

The Issue: When expired reagents are scanned or manually entered, the system will...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2025· Abbott Laboratories

Recalled Item: Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number:...

The Issue: When expired reagents are scanned or manually entered, the system will...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2025· Abbott Laboratories

Recalled Item: Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number:...

The Issue: When expired reagents are scanned or manually entered, the system will...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2025· Abbott Laboratories

Recalled Item: Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number:...

The Issue: When expired reagents are scanned or manually entered, the system will...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2025· Abbott Laboratories

Recalled Item: Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number:...

The Issue: When expired reagents are scanned or manually entered, the system will...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2025· Beckman Coulter Inc.

Recalled Item: DxC 500 AU Clinical Chemistry Analyzer Recalled by Beckman Coulter Inc. Due...

The Issue: The reason for the recall is incorrect sample barcode identification and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2025· Abbott

Recalled Item: Amplatzer TorqVue LP Delivery System (TVLP) Recalled by Abbott Due to Device...

The Issue: Device may have a small breach in the proximal end of the shaft under the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2025· Abbott

Recalled Item: Amplatzer TorqVue LP Catheter (TVLPC) Recalled by Abbott Due to Device may...

The Issue: Device may have a small breach in the proximal end of the shaft under the...

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

Class II — Potential Health HazardOngoing