Product Recalls in New York

Product recalls affecting New York — including food, drugs, consumer products, medical devices, and vehicles distributed to New York. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,659 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,659 in last 12 months

Showing 2420124220 of 55,896 recalls

Medical DeviceJune 27, 2019· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Insulin pump Recalled by Medtronic MiniMed Due to...

The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Medtronic MiniMed

Recalled Item: MiniMed Paradigm 512 Insulin pump Recalled by Medtronic MiniMed Due to The...

The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Medtronic MiniMed

Recalled Item: MiniMed Paradigm Insulin pump Recalled by Medtronic MiniMed Due to The...

The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Insulin pump Recalled by Medtronic MiniMed Due to...

The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Medtronic MiniMed

Recalled Item: MiniMed Paradigm Model 511 Insulin Pump Recalled by Medtronic MiniMed Due to...

The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Insulin pump Recalled by Medtronic MiniMed Due to...

The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Insulin pump Recalled by Medtronic MiniMed Due to...

The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Veo Insulin pump Recalled by Medtronic MiniMed...

The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Insulin pump Recalled by Medtronic MiniMed Due to...

The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Insulin pump Recalled by Medtronic MiniMed Due to...

The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Medtronic MiniMed

Recalled Item: Medtronic MiniMed Paradigm Insulin pump Recalled by Medtronic MiniMed Due to...

The Issue: The action is being initiated due to potential cybersecurity vulnerabilities...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2019· Agfa N.V.

Recalled Item: AGFA Digital Radiography X- Ray system DR 800 with MUSICA Recalled by Agfa...

The Issue: The exposed area of fluo exams possibly does not match the active area of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2019· MicroAire Surgical Instruments, LLC

Recalled Item: SmartRelease Endoscopic Carpal Tunnel Release Handpiece (ECTR handpiece)...

The Issue: There was a higher than normal incidence rate of the blade not retracting...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: Go-EZ Screw 6.5x95 Recalled by BioPro, Inc. Due to Manufacturing flaw in the...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: Go-EZ Screw 6.5x30 Recalled by BioPro, Inc. Due to Manufacturing flaw in the...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: Go-EZ Screw 6.5x120 Recalled by BioPro, Inc. Due to Manufacturing flaw in...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: K-Wire Single Trocar 1.1x150mm Recalled by BioPro, Inc. Due to Manufacturing...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: K-Wire Single Trocar 1.6x150mm Recalled by BioPro, Inc. Due to Manufacturing...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: Go-EZ Screw 6.5x36 Recalled by BioPro, Inc. Due to Manufacturing flaw in the...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: K-Wire Single Trocar 2.5x150mm Recalled by BioPro, Inc. Due to Manufacturing...

The Issue: Manufacturing flaw in the sterile barrier system

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

Class II — Potential Health HazardOngoing