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 2330123320 of 52,339 recalls

Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: AngioDynamics Solero Microwave Tissue Ablation (MTA) System: (1) Solero...

The Issue: Updated Warning Statements in the Operator's Manual/Directions for Use and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: AngioDynamics Solero Microwave Tissue Ablation (MTA) System: (1)Solero...

The Issue: Updated Warning Statements in the Operator's Manual/Directions for Use and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: AngioDynamics Solero Microwave Tissue Ablation (MTA) System: Solero...

The Issue: Updated Warning Statements in the Operator's Manual/Directions for Use and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2019· Remel Inc

Recalled Item: Thio Med w/Dex Recalled by Remel Inc Due to Potential for products to fail...

The Issue: Potential for products to fail performance testing per the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2019· Zimmer Surgical Inc

Recalled Item: Zimmer Biomet Alvarado Knee Holder Base Plate Assembly and Foot Piece...

The Issue: Foreign Material in the Alvarado Knee Holder Base Plate Assembly and Foot...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2019· Ad-Tech Medical Instrument Corporation

Recalled Item: AD-TECH Spencer Probe Depth Electrode Product Usage: The Ad-Tech Depth...

The Issue: An Ad-Tech Clinical Specialist, attended a case on April 15, 2019. During...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2019· Med Tec Inc

Recalled Item: CIVCO Solstice(TM) SRS Immobilization System Recalled by Med Tec Inc Due to...

The Issue: There is a potential for movement of the Solstice Tilting Head Fixation...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2019· Hitachi America, Ltd., Power Systems Division

Recalled Item: PROBEAT-V Recalled by Hitachi America, Ltd., Power Systems Division Due to...

The Issue: There is a potential for a discrepant target position when using 3D3D...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2019· Abbott Gmbh & Co. KG

Recalled Item: Alinity c Cuvette Segments Recalled by Abbott Gmbh & Co. KG Due to...

The Issue: Individual cuvettes within the Alinity c Cuvette Segment may become seated...

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

Class II — Potential Health HazardOngoing
FoodApril 15, 2019· Jensen Tuna Inc

Recalled Item: Frozen ground tuna Recalled by Jensen Tuna Inc Due to Potential Salmonella...

The Issue: Potential to be contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 14, 2019· Schreiber Foods Inc

Recalled Item: Shredded and blocks of Colby & Monterey Jack cheese - Recalled by Schreiber...

The Issue: Product is being recalled due to the presence of foreign material (hard...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 14, 2019· Schreiber Foods Inc

Recalled Item: Great Value Recalled by Schreiber Foods Inc Due to Foreign Object Contamination

The Issue: Product is being recalled due to the presence of foreign material (hard...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 12, 2019· OMNIlife science Inc.

Recalled Item: OMNIBotics iBlock Cutting Guide Recalled by OMNIlife science Inc. Due to The...

The Issue: The OMNIBotics iBlock Cutting Guide does not lock onto the iBlock Saw Guide...

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

Class II — Potential Health HazardOngoing