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. 2,582 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,582 in last 12 months

Showing 2750127520 of 52,339 recalls

DrugMarch 2, 2018· Renaissance Lakewood, LLC

Recalled Item: Flucanazole Injection Recalled by Renaissance Lakewood, LLC Due to...

The Issue: Superpotent and Failed Stability Specifications; out of specification...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 2, 2018· Getinge Disinfection Ab

Recalled Item: Getinge AGS Recalled by Getinge Disinfection Ab Due to There is potential...

The Issue: There is potential for a cart with disinfected goods to unload without the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2018· Getinge Disinfection Ab

Recalled Item: Getinge AGS Recalled by Getinge Disinfection Ab Due to There is potential...

The Issue: There is potential for a cart with disinfected goods to unload without the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2018· Randox Laboratories Ltd.

Recalled Item: Lipase Recalled by Randox Laboratories Ltd. Due to Randox has now released...

The Issue: Randox has now released further steps to avoid contamination of the Lipase...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2018· Beckman Coulter Inc.

Recalled Item: BECKMAN COULTER iChemVELOCITY Recalled by Beckman Coulter Inc. Due to...

The Issue: Beckman Coulter has determined that there is a potential for incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· ICU Medical de Mexico, S.A. de C.V.

Recalled Item: 10" Smallbore Ext Set w/6-Port NanoClave Manifold (Orange Recalled by ICU...

The Issue: ICU Medical is expanding the scope of their previously initiated recall to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· Draeger Medical, Inc.

Recalled Item: Fabius GS Premium Recalled by Draeger Medical, Inc. Due to The automatic...

The Issue: The automatic ventilation may fail if the position detection of the motor is...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2018· Draeger Medical, Inc.

Recalled Item: Fabius MRI Recalled by Draeger Medical, Inc. Due to The automatic...

The Issue: The automatic ventilation may fail if the position detection of the motor is...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2018· ICU Medical de Mexico, S.A. de C.V.

Recalled Item: 18 cm (7") PUR Smallbore Ext Set w/6-Port NanoClave Manifold Recalled by ICU...

The Issue: ICU Medical is expanding the scope of their previously initiated recall to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer M/L Taper Hip Prosthesis Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Certain packages labeled as size 7.5 Extended Offset Reduced Neck length hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· ICU Medical de Mexico, S.A. de C.V.

Recalled Item: 43 cm (17") Smallbore Ext Set w/3-Port NanoClave Manifold Recalled by ICU...

The Issue: ICU Medical is expanding the scope of their previously initiated recall to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· bioMerieux, Inc.

Recalled Item: VIDAS LH Recalled by bioMerieux, Inc. Due to Several complaints were...

The Issue: Several complaints were received for invalid calibration with low calibrator...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· ICU Medical de Mexico, S.A. de C.V.

Recalled Item: 61 cm (24") Smallbore Ext Set w/6-Port NanoClave Manifold Recalled by ICU...

The Issue: ICU Medical is expanding the scope of their previously initiated recall to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· ICU Medical de Mexico, S.A. de C.V.

Recalled Item: PROXIMALE - 18 cm (7") Appx 0.92 ml Recalled by ICU Medical de Mexico, S.A....

The Issue: ICU Medical is expanding the scope of their previously initiated recall to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· ICU Medical de Mexico, S.A. de C.V.

Recalled Item: 216 cm (85") PVC/PUR Smallbore Bifuse Ext Set w/3-Port NanoClave Manifold...

The Issue: ICU Medical is expanding the scope of their previously initiated recall to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer M/L Taper Hip Prosthesis Recalled by Zimmer Biomet, Inc. Due to...

The Issue: Certain packages labeled as size 7.5 Extended Offset Reduced Neck length hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· ICU Medical de Mexico, S.A. de C.V.

Recalled Item: 11" Smallbore Ext Set w/NanoClave Recalled by ICU Medical de Mexico, S.A. de...

The Issue: ICU Medical is expanding the scope of their previously initiated recall to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· ICU Medical de Mexico, S.A. de C.V.

Recalled Item: 191 cm (75") Appx 2.9 ml Recalled by ICU Medical de Mexico, S.A. de C.V. Due...

The Issue: ICU Medical is expanding the scope of their previously initiated recall to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· ICU Medical de Mexico, S.A. de C.V.

Recalled Item: Kit w/3 Ext Sets Recalled by ICU Medical de Mexico, S.A. de C.V. Due to ICU...

The Issue: ICU Medical is expanding the scope of their previously initiated recall to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· ICU Medical de Mexico, S.A. de C.V.

Recalled Item: 6" Smallbore Ext Set w/6-Port NanoClave Manifold Recalled by ICU Medical de...

The Issue: ICU Medical is expanding the scope of their previously initiated recall to...

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

Class II — Potential Health HazardOngoing