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. 2,406 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,406 in last 12 months

Showing 4394143960 of 52,339 recalls

Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: LIPOSUCTION PACK AESTHETIC SURG.CENTER CONTENTS: (1) BLADE SURG. #11 CARBON...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: Tummy Tuck Pack- FJG Recalled by Customed, Inc Due to Customed has...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: LAPAROTOMY PACK BASIC CODE 900-2829 CONTENTS: (2) TOWELS ABSORBENT 15"...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: ORTHO IMPLANT SURGICAL PACK - (1) CAUTERY TIP POLISHER (1) Recalled by...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: KNEE ARTHROSCOPY PACK 4 CUSTOMED CONTENTS: (1) COVER TABLE REINFORCED...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: CESAREAN PACK- (1) COVER TABLE REINFORCED 50" X 90" (2) Recalled by...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: LAPAROSCOPY PREMIUM PACK - (1) TABLE COVER REINFORCED 50" x Recalled by...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: ANGIOGRAPHY PACK - ( 1) FEMORAL ANGlO. DRAPE WITH POUCH Recalled by...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 20, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: syngo Lab Data Manager Recalled by Siemens Healthcare Diagnostics, Inc. Due...

The Issue: Certain configuration parameters may cause the ranges to not hold results as...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2014· Customed, Inc

Recalled Item: UROLOGY PACK- (2) SYRINGE 30ML SLIP TIP 1 ML LIF Recalled by Customed, Inc...

The Issue: Customed has determined that there is the possibility that packaging...

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

Class I — Serious Health HazardOngoing
DrugMay 20, 2014· West-Ward Pharmaceutical Corp.

Recalled Item: Isoniazid Tablets Recalled by West-Ward Pharmaceutical Corp. Due to Failed...

The Issue: Failed Dissolution Specifications: Stability lots cannot support dissolution...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 19, 2014· KCI USA, Inc.

Recalled Item: CelluTome Epidermal Harvesting System Part number CT-H25 or Part Number...

The Issue: Blade can shift during shipping which makes the product ineffective.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Integra LifeSciences Corp.

Recalled Item: Accell Evo3C Demineralized Bone Matrix Recalled by Integra LifeSciences...

The Issue: This lot of Accell Evo3C Demineralized Bone Matrix, 5cc was incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...

The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...

The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...

The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...

The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...

The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Small Bone Innovations

Recalled Item: Small Bone Innovations 3.0/4.0mm AutoFIX" Cannulated Compression Screw...

The Issue: Small Bone Innovations (SBi) is recalling all lots of 3.0/4.0mm AutoFIX"...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2014· Zimmer, Inc.

Recalled Item: NexGen Complete Knee Solution Recalled by Zimmer, Inc. Due to Zimmer is...

The Issue: Zimmer is initiating a voluntary recall of specific identified lots due to...

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

Class II — Potential Health HazardOngoing