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. 1,772 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
1,772 in last 12 months

Showing 4182141840 of 52,339 recalls

Medical DeviceNovember 21, 2014· Smiths Medical ASD, Inc.

Recalled Item: Hypodermic Needle Pro¿ Edge" Safety Device with Syringe 20G x1 Recalled by...

The Issue: Needle is not captured in the needle safety sheath in specific lots.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2014· Zimmer Manufacturing B.V.

Recalled Item: Bone Screw Recalled by Zimmer Manufacturing B.V. Due to Analysis of returned...

The Issue: Analysis of returned complaint devices, product in inventory, and device...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2014· TomoTherapy Incorporated

Recalled Item: TomoTherapy Treatment System with software versions 2.0.1 / 2.0.2 / Recalled...

The Issue: Accuray has become aware of a potential safety issue related to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2014· Teleflex, Inc.

Recalled Item: Bronchial Double Lumen Tube Set (Right) Recalled by Teleflex, Inc. Due to...

The Issue: Customer complaints reporting that the cobb connector detached from the main...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2014· Teleflex, Inc.

Recalled Item: Tracheopart Set (Right) Recalled by Teleflex, Inc. Due to Customer...

The Issue: Customer complaints reporting that the cobb connector detached from the main...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2014· Teleflex, Inc.

Recalled Item: Carlens Bronchial Double Lumen Tube Set (Left) Sterile Recalled by Teleflex,...

The Issue: Customer complaints reporting that the cobb connector detached from the main...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2014· Teleflex, Inc.

Recalled Item: Bronchial Double Lumen Tube Set (Left) Recalled by Teleflex, Inc. Due to...

The Issue: Customer complaints reporting that the cobb connector detached from the main...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2014· Teleflex, Inc.

Recalled Item: White Bronchial Double Lumen Tube Set (Right) Sterile Recalled by Teleflex,...

The Issue: Customer complaints reporting that the cobb connector detached from the main...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2014· Teleflex, Inc.

Recalled Item: Bronchial One Lumen Tube - Right Recalled by Teleflex, Inc. Due to Customer...

The Issue: Customer complaints reporting that the cobb connector detached from the main...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2014· Becton Dickinson & Co.

Recalled Item: BBL Port A Cul tubes Recalled by Becton Dickinson & Co. Due to The products...

The Issue: The products may exhibit indications of excessive oxidation. Excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2014· Becton Dickinson & Co.

Recalled Item: BBL Port A Cul tubes with Swabs Sterile Pack Recalled by Becton Dickinson &...

The Issue: The products may exhibit indications of excessive oxidation. Excessive...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2014· Teleflex, Inc.

Recalled Item: Bronchial One Lumen Tube - Left Recalled by Teleflex, Inc. Due to Customer...

The Issue: Customer complaints reporting that the cobb connector detached from the main...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2014· Teleflex, Inc.

Recalled Item: Tracheopart Set (Left) Recalled by Teleflex, Inc. Due to Customer complaints...

The Issue: Customer complaints reporting that the cobb connector detached from the main...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2014· Teleflex, Inc.

Recalled Item: Bronchial Double Lumen Tube Set (Left) Recalled by Teleflex, Inc. Due to...

The Issue: Customer complaints reporting that the cobb connector detached from the main...

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

Class II — Potential Health HazardOngoing
FoodNovember 20, 2014· Evershing International Trading Inc.

Recalled Item: Wake-Up Instant Coffee Mix (weasel coffee) Melange de Cafe Instantane...

The Issue: Firm was notified by CFIA and FDA that CFIA testing found undeclared milk...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender I 17/60 10 pieces Product Usage: Intended for Recalled by...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender II 17/80 10 + 10 pieces Product Usage: Recalled by Roche...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender II 13/80 10 + 10 pieces Product Usage: Recalled by Roche...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender I 17/110 10 pieces Product Usage: Intended for Recalled by...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender I 17/80 10 pieces Product Usage: Intended for Recalled by...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing