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. 1,108 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
1,108 in last 12 months

Showing 11941–11960 of 29,228 recalls

Medical DeviceApril 30, 2020· Medtronic Inc.

Recalled Item: MiniMed 630G with SmartGuard Recalled by Medtronic Inc. Due to Missing...

The Issue: Missing solder battery connection, which could interrupt power of insulin pump.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Medtronic Inc.

Recalled Item: MiniMed 670G Recalled by Medtronic Inc. Due to Missing solder battery...

The Issue: Missing solder battery connection, which could interrupt power of insulin pump.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Normand-Info S.A.S.U.

Recalled Item: Remisol Advance running Software Version 1.12 The Normand Info Remisol...

The Issue: Results from repeated run for WBC (White Bloodcell Count), UWBC (Urine Whit...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Medtronic Inc.

Recalled Item: MiniMed 640G Recalled by Medtronic Inc. Due to Missing solder battery...

The Issue: Missing solder battery connection, which could interrupt power of insulin pump.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 400mL Recalled by Covidien Llc Due to Temperature sensing catheters...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 100% Silicone Silver-Hydrogel Coated Premium Urine Meter Foley Tray...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 400 ml 100% Silicone Silver-Hydrogel Coated Premium Urine Meter Foley...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 100% Silicone Silver-Hydrogel Coated Foley Catheter with Temperature...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 100% Silicone Premium Urine Meter Tray 400mL Recalled by Covidien Llc...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2020· Covidien Llc

Recalled Item: Dover 400 ml 100% Silicone Silver-Hydrogel Coated Premium Urine Meter Foley...

The Issue: Temperature sensing catheters failed to meet the established calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2020· GE Healthcare, LLC

Recalled Item: Giraffe Incubator with installed Servo Oxygen module. Infant incubator....

The Issue: Potential for certain Giraffe Incubators and Giraffe OmniBeds to deliver a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2020· GE Healthcare, LLC

Recalled Item: Giraffe OmniBed with installed Servo Oxygen module. Infant incubator and...

The Issue: Potential for certain Giraffe Incubators and Giraffe OmniBeds to deliver a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2020· Defibtech, LLC

Recalled Item: DDU-2400EN Lifeline PRO Recalled by Defibtech, LLC Due to A component issue...

The Issue: A component issue may cause the AED to abort a shock delivery or reset...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2020· Defibtech, LLC

Recalled Item: DDU-2450 Lifeline ECG Model Numbers DDU-A2450EN DDU-E2450DE DDU-E2450EN...

The Issue: A component issue may cause the AED to abort a shock delivery or reset...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2020· Philips North America, LLC

Recalled Item: Philips HeartStart MRx Monitor/Defibrillators Model numbers M3535A Recalled...

The Issue: HeartStart XL MonitorlDefibrillators may not have been included in prior...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2020· Defibtech, LLC

Recalled Item: DDU-2300 Lifeline/ReviveR View Recalled by Defibtech, LLC Due to A component...

The Issue: A component issue may cause the AED to abort a shock delivery or reset...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Sterile Disposable Connectors ASY 1/4 X 3/8 REDUCER W/LL 24. Recalled by...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Sterile Disposable Connectors ASY STR CONN 3/16 STRLE 24. REF/ Recalled by...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Sterile Disposable Connectors ASY ASY STR CONN 3/8 STRLE 24 Recalled by...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Vein Irrigation Cannula with blunt tip. ASY BIC Recalled by LivaNova USA...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing