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. 1,035 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
1,035 in last 12 months

Showing 26701–26720 of 53,528 recalls

Medical DeviceJuly 13, 2018· Philips Electronics North America Corporation

Recalled Item: Philips SureSigns VM 3/4/6/8 Patient Monitors Recalled by Philips...

The Issue: Philips has received several reports in which monitors with lithium ion...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2018· Philips Electronics North America Corporation

Recalled Item: Philips SureSigns VSV (Vital Signs Viewer) Recalled by Philips Electronics...

The Issue: Philips has received several reports in which monitors with lithium ion...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2018· Philips Electronics North America Corporation

Recalled Item: Philips SureSigns VS4 Vital Signs Monitor Recalled by Philips Electronics...

The Issue: Philips has received several reports in which monitors with lithium ion...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2018· Philips Electronics North America Corporation

Recalled Item: Philips SureSigns VS2 monitor Recalled by Philips Electronics North America...

The Issue: Philips has received several reports in which monitors with lithium ion...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2018· Philips Electronics North America Corporation

Recalled Item: Philips SureSigns VS3 Vital Signs Monitor Recalled by Philips Electronics...

The Issue: Philips has received several reports in which monitors with lithium ion...

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

Class II — Potential Health HazardOngoing
DrugJuly 12, 2018· Sun Pharmaceutical Industries, Inc.

Recalled Item: Testosterone Cypionate Injection Recalled by Sun Pharmaceutical Industries,...

The Issue: Presence of Particulate Matter: organic and inorganic compounds detected in...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 12, 2018· GE Healthcare, LLC

Recalled Item: Revolution CT systems with the SmartStep Option The system is Recalled by GE...

The Issue: On the Revolution CT systems equipped with the SmartStep Option, the Z...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Ultradent Products, Inc.

Recalled Item: Enamelast Cool Mint/OT Varnish 5% NaF Mint Label Enamelast Unit Recalled by...

The Issue: Dental varnish has the possibility of having an unpleasant and off flavor.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Orthosensor, Inc.

Recalled Item: OrthoSensor VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Right Recalled...

The Issue: Some sensors were reported to have fluid inside the posterior lateral corner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Orthosensor, Inc.

Recalled Item: OrthoSensor VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Left Recalled by...

The Issue: Some sensors were reported to have fluid inside the posterior lateral corner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Orthosensor, Inc.

Recalled Item: OrthoSensor VERASENSE for Zimmer Biomet Persona CR G-H/7-12 Right Recalled...

The Issue: Some sensors were reported to have fluid inside the posterior lateral corner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Orthosensor, Inc.

Recalled Item: OrthoSensor VERASENSE for Zimmer Biomet Persona CR C-D/3-9 Right Recalled by...

The Issue: Some sensors were reported to have fluid inside the posterior lateral corner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Orthosensor, Inc.

Recalled Item: OrthoSensor VERASENSE for Zimmer Biomet Persona CR C-D/3-9 Left Recalled by...

The Issue: Some sensors were reported to have fluid inside the posterior lateral corner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Orthosensor, Inc.

Recalled Item: OrthoSensor VERASENSE for Zimmer Biomet Persona CR G-H/7-12 Left Recalled by...

The Issue: Some sensors were reported to have fluid inside the posterior lateral corner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Ortho Clinical Diagnostics Inc

Recalled Item: VITROS Immunodiagnostic Products - Folate Reagent Pack(10758750009237)...

The Issue: The recalling firm determined that biased results may occur for specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Ortho Clinical Diagnostics Inc

Recalled Item: VITROS Immunodiagnostic Products - FSH Reagent Pack (10758750000302) 1931922...

The Issue: The recalling firm determined that biased results may occur for specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Ortho Clinical Diagnostics Inc

Recalled Item: VITROS Immunodiagnostic Products - Prolactin Reagent Pack (10758750000111)...

The Issue: The recalling firm determined that biased results may occur for specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Ortho Clinical Diagnostics Inc

Recalled Item: VITROS Immunodiagnostic Products - TSH Reagent Pack (10758750000227) 1912997...

The Issue: The recalling firm determined that biased results may occur for specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Medical Components, Inc dba MedComp

Recalled Item: Duo-Flow XTP Straight Full Set Recalled by Medical Components, Inc dba...

The Issue: The suture wings have the potential to crack or break. Potential patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Medical Components, Inc dba MedComp

Recalled Item: Duo-Flow Catheter Full Tray Recalled by Medical Components, Inc dba MedComp...

The Issue: The suture wings have the potential to crack or break. Potential patient...

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

Class II — Potential Health HazardOngoing