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. 1,171 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
1,171 in last 12 months

Showing 1781–1800 of 53,528 recalls

Medical DeviceAugust 4, 2025· Merit Medical Systems, Inc.

Recalled Item: PhD Hemostasis Valve Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Hemostasis valve has a manufacturing defect and when used the valve cap may...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Azurion System configured with a 1 Phase UPS. Azurion family (R1.x...

The Issue: Philips Azurion and Allura systems configured with a 1 Phase Uninterruptible...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Allura System configured with a 1 Phase UPS. Allura family (R1.x...

The Issue: Philips Azurion and Allura systems configured with a 1 Phase Uninterruptible...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Interventional Fluoroscopic X-Ray System - Philips Allura Xper Series....

The Issue: Potential that a component (air baffle) may be missing in some Nehalem...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2025· Medline Industries, LP

Recalled Item: Reprocessed ACUSON AcuNav Ultrasound Catheter for intracardiac and...

The Issue: Specific lots of reprocessed electrophysiology and ultrasound catheters may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 31, 2025· Medline Industries, LP

Recalled Item: Reprocessed Inquiry Steerable Diagnostics Catheter for electrogram recording...

The Issue: Specific lots of reprocessed electrophysiology and ultrasound catheters may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 31, 2025· Medline Industries, LP

Recalled Item: Reprocessed Webster CS Catheter 10 Electrodes for electrophysiological...

The Issue: Specific lots of reprocessed electrophysiology and ultrasound catheters may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 31, 2025· Lumicell, Inc.

Recalled Item: Brand Name: 900-00218 Sterile Cover 10-Pack Shipper Box Assembly Product...

The Issue: The potential of the elastic bands included in the kit detaching or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2025· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: LinkSymphoKnee System Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due...

The Issue: Some modular LinkSymphoKnee TiNbN Tibial Components were manufactured with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2025· Medline Industries, LP

Recalled Item: Reprocessed ViewFlex Xtra ICE Catheter to visualize cardiac structures...

The Issue: Specific lots of reprocessed electrophysiology and ultrasound catheters may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 31, 2025· Medline Industries, LP

Recalled Item: Reprocessed Livewire Steerable Electrophysiology Catheter Item Numbers...

The Issue: Specific lots of reprocessed electrophysiology and ultrasound catheters may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 30, 2025· S.I.N. Implant System Ltda

Recalled Item: IMPLANT EPIKUT PLUS MT16 3 Recalled by S.I.N. Implant System Ltda Due to...

The Issue: Dental implants were imported under temperature and storage conditions that...

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

Class II — Potential Health HazardOngoing
DrugJuly 30, 2025· Exela Pharma Sciences LLC

Recalled Item: 4.2% Sodium Bicarbonate Injection Recalled by Exela Pharma Sciences LLC Due...

The Issue: Failed Impurities/Degradation Specifications: out of specification results...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 30, 2025· GenoGenix LLC

Recalled Item: Ultra Burn for Injection Recalled by GenoGenix LLC Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 30, 2025· GenoGenix LLC

Recalled Item: Semaglutide with B12 for Injection Recalled by GenoGenix LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 30, 2025· GenoGenix LLC

Recalled Item: Sterile Saline Reconstitution Solution for Injection Recalled by GenoGenix...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 30, 2025· GenoGenix LLC

Recalled Item: B6 (Pyridoxine HCl) for Injections Recalled by GenoGenix LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 30, 2025· GenoGenix LLC

Recalled Item: Sermorelin Lyophilized powder for reconstitution Recalled by GenoGenix LLC...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 30, 2025· GenoGenix LLC

Recalled Item: BPC-157/Thymosin Beta-4 for Injection Recalled by GenoGenix LLC Due to Lack...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 30, 2025· GenoGenix LLC

Recalled Item: Low Solubility Peptide Reconstitution Solution for Injection Recalled by...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund