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 31013120 of 29,228 recalls

Medical DeviceAugust 30, 2024· Blue Ortho

Recalled Item: Predict+ is a data-driven Recalled by Blue Ortho Due to Predict+ is being...

The Issue: Predict+ is being recalled for lack of pre-market clearance/approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT Recalled by MEDLINE...

The Issue: It has been determined that certain Blood Pressure Monitors containing a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· Fresenius Kabi USA, LLC

Recalled Item: Ivenix Infusion System (IIS) Recalled by Fresenius Kabi USA, LLC Due to The...

The Issue: The software has anomalies that have the potential to cause alarms,...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 30, 2024· Merit Medical Systems, Inc.

Recalled Item: Melrose Wakefield Hospital Injector And Syringe Recalled by Merit Medical...

The Issue: Due to a manufacturing process resulting in holes/breaches in the Tyvek...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT Recalled by MEDLINE...

The Issue: It has been determined that certain Blood Pressure Monitors containing a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· Merit Medical Systems, Inc.

Recalled Item: Monarch Inflation Device 30 atm/bar MAP152 AssessPLUS Large Bore Hemostasis...

The Issue: Due to a manufacturing process resulting in holes/breaches in the Tyvek...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· Merit Medical Systems, Inc.

Recalled Item: Monarch Inflation Device 30 atm/bar Injector And Syringe Recalled by Merit...

The Issue: Due to a manufacturing process resulting in holes/breaches in the Tyvek...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· Merit Medical Systems, Inc.

Recalled Item: Monarch Inflation Device 30 atm/bar MAP302 Honor Hemostasis Valve Metal...

The Issue: Due to a manufacturing process resulting in holes/breaches in the Tyvek...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE Automatic Digital Blood Pressure Monitor Recalled by MEDLINE...

The Issue: It has been determined that certain Blood Pressure Monitors containing a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2024· Merit Medical Systems, Inc.

Recalled Item: Monarch Inflation Device MAP 112 Access-9 Large Bore Hemostasis Value...

The Issue: Due to a manufacturing process resulting in holes/breaches in the Tyvek...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2024· Tornier, Inc

Recalled Item: stryker TORNIER PERFORM HUMERAL SYSTEM - STEMLESS US Anatomic Nucleus...

The Issue: One lot of Perform Humeral Nucleus may exceed the specification for...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2024· CooperVision, Inc.

Recalled Item: BIOFINITY XR TORIC Lenses - Soft Contact lenses Indicated for Recalled by...

The Issue: Manufactured with a misaligned axis resulting in lenses with the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2024· Tornier, Inc

Recalled Item: Stryker Tornier Perform Humeral System Recalled by Tornier, Inc Due to...

The Issue: Devices from one lot of Perform" Reversed Inserts may contain a locking ring...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2024· CooperVision, Inc.

Recalled Item: Biofinity Toric Multifocal Lenses - Soft Contact lenses Indicated for...

The Issue: Manufactured with a misaligned axis resulting in lenses with the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2024· Wilson-Cook Medical Inc.

Recalled Item: Cook Medical Hemo-7 Hemospray Endoscopic Hemostat Recalled by Wilson-Cook...

The Issue: Specific lots of product have been manufactured with nonconforming raw...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2024· Microcare Medical

Recalled Item: Good Vibrations Ultrasonic Cleaner Solution Recalled by Microcare Medical...

The Issue: Contaminated equipment and packaging caused Klebsiella oxytoca, Enterobacter...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE OPEN HEART Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Medline Industries, LP. has identified certain kits containing the recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE HEART OVERHEAD TABLE PACK Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Medline Industries, LP. has identified certain kits containing the recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Sterile Laparoscopy Pack Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: CONMED Corporation (vendor) initiated a recall for select lot numbers of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE OPEN HEART PACK Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: Medline Industries, LP. has identified certain kits containing the recalled...

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

Class II — Potential Health HazardOngoing