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. 2,764 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,764 in last 12 months

Showing 65416560 of 29,154 recalls

Medical DeviceMay 8, 2023· Galt Medical Corporation

Recalled Item: Tearaway Introducer Set Recalled by Galt Medical Corporation Due to Sheath...

The Issue: Sheath introducer assemblies could potentially, due to improper storage...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2023· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Calibrator Kit 20-in vitro diagnostic use only....

The Issue: Potential to cause biased results in the upper end of the reportable range...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2023· Vyaire Medical

Recalled Item: bellavista 1000 Ventilator Recalled by Vyaire Medical Due to Vyaire Medical...

The Issue: Vyaire Medical identified two patient safety risks during the use of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2023· Vyaire Medical

Recalled Item: bellavista 1000e Ventilator Recalled by Vyaire Medical Due to Vyaire Medical...

The Issue: Vyaire Medical identified two patient safety risks during the use of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2023· T.A.G. MEDICAL PRODUCTS CORPORATION, LTD.

Recalled Item: BETTA LINK LG KNOTLESS IMPLANT KIT-Intended for use in soft Recalled by...

The Issue: Drill guides might bend when axial forces are applied by surgeon during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2023· Olympus Corporation of the Americas

Recalled Item: Single Use Repositionable Clip QUICKCLIP PRO 165CM 5/BX- Intended for...

The Issue: Complaints on clip deployment occurring during clinical procedures, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2023· T.A.G. MEDICAL PRODUCTS CORPORATION, LTD.

Recalled Item: Betta Link LG Reusable ProngED Guide - Intended for use Recalled by T.A.G....

The Issue: Drill guides might bend when axial forces are applied by surgeon during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2023· Olympus Corporation of the Americas

Recalled Item: Single Use Repositionable Clip QUICKCLIP PRO 230CM 5/BX- Intended for...

The Issue: Complaints on clip deployment occurring during clinical procedures, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2023· T.A.G. MEDICAL PRODUCTS CORPORATION, LTD.

Recalled Item: Betta Link LG Reusable Fishmouth Guide-Intended for use in soft Recalled by...

The Issue: Drill guides might bend when axial forces are applied by surgeon during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2023· T.A.G. MEDICAL PRODUCTS CORPORATION, LTD.

Recalled Item: BETTA LINK SR REUSABLE PRONGED GUIDE- Intended for use in Recalled by T.A.G....

The Issue: Drill guides might bend when axial forces are applied by surgeon during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2023· Olympus Corporation of the Americas

Recalled Item: Single Use Repositionable Clip QUICKCLIP PRO 230 CM 10/BX- Intended Recalled...

The Issue: Complaints on clip deployment occurring during clinical procedures, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2023· T.A.G. MEDICAL PRODUCTS CORPORATION, LTD.

Recalled Item: BETTA LINK SR KNOTLESS IMPLANT KIT-Intended for use in soft Recalled by...

The Issue: Drill guides might bend when axial forces are applied by surgeon during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2023· T.A.G. MEDICAL PRODUCTS CORPORATION, LTD.

Recalled Item: BETTA LINK SR REUSABLE FISHMOUTH GUIDE-Intended for use in soft Recalled by...

The Issue: Drill guides might bend when axial forces are applied by surgeon during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2023· Olympus Corporation of the Americas

Recalled Item: Single Use Repositionable Clip QUICKCLIP PRO 165 CM 10/BX- Intended Recalled...

The Issue: Complaints on clip deployment occurring during clinical procedures, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2023· NOXBOX LTD

Recalled Item: NOxBOXi Nitric Oxide Delivery System Recalled by NOXBOX LTD Due to Device...

The Issue: Device may experience malfunctions due to misalignment of the check valve in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 3, 2023· Bolton Medical Inc.

Recalled Item: The TREO ABDOMINAL STENT-GRAFT SYSTEM (TREO) consists of four types of...

The Issue: Potential for the incorrect size stent-graft than the printed carton label.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE THERAHONEY GEL Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: Medline issued a recall on TheraHoney Wound Gel due to the manufacturer...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2023· Smith & Nephew, Inc.

Recalled Item: Smith&Nephew ENGAGE Cementless Partial Knee System Recalled by Smith &...

The Issue: Recent complaint data indicates that the revision rate may be trending...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2023· Smith & Nephew, Inc.

Recalled Item: Smith&Nephew ENGAGE Cementless Partial Knee System Recalled by Smith &...

The Issue: Recent complaint data indicates that the revision rate may be trending...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2023· Smith & Nephew, Inc.

Recalled Item: Smith&Nephew ENGAGE Cementless Partial Knee System Recalled by Smith &...

The Issue: Recent complaint data indicates that the revision rate may be trending...

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

Class II — Potential Health HazardOngoing