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 28212840 of 29,228 recalls

Medical DeviceOctober 7, 2024· Philips Respironics, Inc.

Recalled Item: Garbin Evo. Model Number: LD2110X23B. Intended for invasive and non-invasive...

The Issue: Potential for in-line nebulizer configuration in certain locations to result...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 7, 2024· Philips Respironics, Inc.

Recalled Item: LifeVent EVO2. Model Number: SP2100X26B. Intended for invasive and...

The Issue: Potential for in-line nebulizer configuration in certain locations to result...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 7, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Zenition 50 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...

The Issue: Potential for the Mains Control Unit board fuse may blow out during system...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy Evo O2. Model Numbers: FP2100X10 Recalled by Philips Respironics,...

The Issue: Potential for in-line nebulizer configuration in certain locations to result...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 7, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy Evo. Model Numbers: DS2110X11B Recalled by Philips Respironics, Inc....

The Issue: Potential for in-line nebulizer configuration in certain locations to result...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 7, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Zenition 70 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...

The Issue: Potential for the Mains Control Unit board fuse may blow out during system...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2024· St. Jude Medical

Recalled Item: CARDIOMEMS HF PRESSURE MEASUREMENT SYSTEM CardioMEMSTM HF System Hosptial...

The Issue: As a result of a cloud data migration of Patient and Hospital Electronic...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2024· St. Jude Medical

Recalled Item: CARDIOMEMS HF PRESSURE MEASUREMENT SYSTEM CardioMEMSTM HF System Patient...

The Issue: As a result of a cloud data migration of Patient and Hospital Electronic...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Hobbs Medical, Inc.

Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...

The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Caire, Inc.

Recalled Item: CAIRE FreeStyle Comfort portable oxygen concentrator Recalled by Caire, Inc....

The Issue: Potential failure of affected units to recharge the battery of the oxygen...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Hobbs Medical, Inc.

Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...

The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Hobbs Medical, Inc.

Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...

The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Hobbs Medical, Inc.

Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...

The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Hobbs Medical, Inc.

Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...

The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Hobbs Medical, Inc.

Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...

The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Caire, Inc.

Recalled Item: CAIRE FreeStyle Comfort portable oxygen concentrator Recalled by Caire, Inc....

The Issue: Potential failure of affected units to recharge the battery of the oxygen...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Hobbs Medical, Inc.

Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...

The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Caire, Inc.

Recalled Item: CAIRE FreeStyle Comfort portable oxygen concentrator Recalled by Caire, Inc....

The Issue: Potential failure of affected units to recharge the battery of the oxygen...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Caire, Inc.

Recalled Item: CAIRE FreeStyle Comfort portable oxygen concentrator Recalled by Caire, Inc....

The Issue: Potential failure of affected units to recharge the battery of the oxygen...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2024· Hobbs Medical, Inc.

Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...

The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...

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

Class II — Potential Health HazardOngoing