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 28812900 of 29,228 recalls

Medical DeviceSeptember 25, 2024· Cardinal Health 200, LLC

Recalled Item: Monoject U-100 1 mL Insulin Syringe Luer-Lock with Tip Cap Soft Pack...

The Issue: Certain lots of listed lots of Cardinal Health Monoject U-100 1 mL Insulin...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 24, 2024· Siemens Healthcare Diagnostics Inc

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

The Issue: Siemens Healthcare Diagnostics Inc. has confirmed that a negative sodium...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 24, 2024· West Pharmaceutical Services AZ, Inc.

Recalled Item: Brand Name: Vial2Bag Advanced¿ Product Name: Vial2Bag Advanced¿ 20mm...

The Issue: Due to packaging damage from heat exposure during shipping/transportation...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2024· Onkos Surgical, Inc.

Recalled Item: ELEOS MALE-FEMALE MIDSECTION 40MM. Part Number: 25001040E. Component of...

The Issue: Potential challenge with intraoperative assembly of the external taper of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG PAT XRAY 3X3 Model/Catalog Number: 801409. The surgical patties...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG PAT XRAY 1/2X1-1/2 Model/Catalog Number: 801404. The surgical patties...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG PAT XRAY 3/4X3/4 Model/Catalog Number: 801401. The surgical patties...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG PAT XRAY 1/4X1/4 Model/Catalog Number: 801399. The surgical patties...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG STRP 1/2X6 Model/Catalog Number: 801451. The surgical patties and...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG STRP 1/8X6 Model/Catalog Number: 801449. The surgical patties and...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG PAT XRAY 1/2X1/2 Model/Catalog Number: 801400. The surgical patties...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG STRP 3/4X6 Model/Catalog Number: 801452. The surgical patties and...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG STRP 2X6 Model/Catalog Number: 801455. The surgical patties and...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG STRP 3X6 Model/Catalog Number: 801456. The surgical patties and...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Remel, Inc

Recalled Item: remel BactiDrop Acridine Orange Recalled by Remel, Inc Due to A color change...

The Issue: A color change of the solution within the dropper can occur from...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG PAT XRAY 1/4X3 Model/Catalog Number: 801398. The surgical patties...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG STRP 3-1/2X6 Model/Catalog Number:801457. The surgical patties and...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG PAT XRAY 1/2X1 Model/Catalog Number: 801402. The surgical patties...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: SURG STRP 1X6-200 Model/Catalog Number: 801453. The surgical patties and...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· Integra LifeSciences Corp.

Recalled Item: MICR PATIE RND Model/Catalog Number: 801396. CODMAN Surgical Patties and...

The Issue: Identified higher-than-expected levels of endotoxin within the raw material...

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

Class II — Potential Health HazardOngoing