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. 2,544 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,544 in last 12 months

Showing 3402134040 of 52,339 recalls

Medical DeviceJuly 15, 2016· Topcon Medical Laser Systems, Inc

Recalled Item: Opthalmic: PASCAL Synthesis is an ophthalmic scanning laser system. The...

The Issue: Topcon discovered an anomaly with titration, only when EpM is turned on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: cobas e411 Immunoassay Analyzer e411: Immunoassay Analyzer Product Usage:...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: cobas 6000 Series system c6000 Recalled by Roche Diagnostics Operations,...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Roche Diagnostics Operations, Inc.

Recalled Item: cobas 6800/8800 system Hepatitis Viral B DNA Detection Product Usage:...

The Issue: Roche has received four reports of injury caused by the sharp edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2016· Ethicon Endo-Surgery Inc

Recalled Item: Endoscopic Articulating Linear Cutter Recalled by Ethicon Endo-Surgery Inc...

The Issue: Quality control identified a component issue where the pinion gear in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2016· Intuitive Surgical, Inc.

Recalled Item: STAPLER Recalled by Intuitive Surgical, Inc. Due to Field failures were...

The Issue: Field failures were reported related to the da Vinci Xi Surgical System...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2016· Intuitive Surgical, Inc.

Recalled Item: STAPLER 30 Recalled by Intuitive Surgical, Inc. Due to Field failures were...

The Issue: Field failures were reported related to the da Vinci Xi Surgical System...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2016· ORTHO-CLINICAL DIAGNOSTICS

Recalled Item: VITROS Immunodiagnostic Products Estradiol Reagent Pack Recalled by...

The Issue: Ortho Clinical Diagnostics has issued a recall of their VITROS...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2016· Straumann Manufacturing, Inc.

Recalled Item: Straumann Bone Level Implant Recalled by Straumann Manufacturing, Inc. Due...

The Issue: Misalignment with the Loxim transfer piece markings, the positioning of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2016· Merge Healthcare, Inc.

Recalled Item: Merge RadSuite Recalled by Merge Healthcare, Inc. Due to It was reported by...

The Issue: It was reported by a customer that RadSuite images are not appearing as...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2016· Intuitive Surgical, Inc.

Recalled Item: CURVED-TIP STAPLER 30 Recalled by Intuitive Surgical, Inc. Due to Field...

The Issue: Field failures were reported related to the da Vinci Xi Surgical System...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2016· Straumann Manufacturing, Inc.

Recalled Item: Straumann Bone Level Implant Recalled by Straumann Manufacturing, Inc. Due...

The Issue: Misalignment with the Loxim transfer piece markings, the positioning of the...

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

Class II — Potential Health HazardOngoing
FoodJuly 14, 2016· Monogram Appetizers, Inc

Recalled Item: Poppers brand Mozzarella Cheese Sticks Net Wt. 32 oz. (2 Recalled by...

The Issue: Monogram Appetizers is recalling Poppers Brand Mozzarella Cheese Sticks...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 14, 2016· Ajinomoto Windsor Inc., Golden Tiger Plant

Recalled Item: Molly's Kitchen Hotzzarella Cheese Sticks Recalled by Ajinomoto Windsor...

The Issue: Ajinomoto Windsor is recalling Cheese Sticks because it may be contaminated...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 13, 2016· ICC/Marie Callender's Products

Recalled Item: Marie Callender's Cheese Biscuit Recalled by ICC/Marie Callender's Products...

The Issue: Firm was notified by supplier that flour used as an ingredient in the cheese...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 13, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS ZEE AND ZEEGO Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: The possibility exists for contaminants, in the form of biomass, to develop...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2016· Diasorin Inc.

Recalled Item: LIAISON Estradiol II Gen Recalled by Diasorin Inc. Due to DiaSorin is...

The Issue: DiaSorin is issuing an urgent medical device correction for the LIAISON¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS Q AND Q.ZEN- MODULAR ANGIOGRAPHIC SYSTEM Recalled by Siemens Medical...

The Issue: The possibility exists for contaminants, in the form of biomass, to develop...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM ARTIS MODULAR ANGIOGRAPHY SYSTEM Recalled by Siemens Medical Solutions...

The Issue: The possibility exists for contaminants, in the form of biomass, to develop...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2016· Resmed Corporation

Recalled Item: Quattro Air FFM MED  AMER Recalled by Resmed Corporation Due to Masks in...

The Issue: Masks in this lot, labelled and sold as 62702 vented Quattro Air FFM size...

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

Class II — Potential Health HazardOngoing