Product Recalls in Arizona

Product recalls affecting Arizona — including food, drugs, consumer products, medical devices, and vehicles distributed to Arizona. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,595 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,595 in last 12 months

Showing 2230122320 of 52,339 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 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
Medical DeviceJune 25, 2019· BioPro, Inc.

Recalled Item: Go-EZ Screw 6.5x110 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: Go-EZ Screw 6.5x32 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 6.5x36 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: Go-EZ Screw 6.5x90 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 6.5x100 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 HBS Sterile Lot 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: Go-EZ Screw 6.5x85 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 6.5x115 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: 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 6.5x105 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 Sterile Single Trochar 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 HBS Sterile 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 Sterile Single Trochar .045 Recalled by BioPro, Inc. Due to...

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 6.5x38 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 6.5x95 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: K-Wire Single Trocar 2.5x170mm 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 6.5x34 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