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. 2,782 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,782 in last 12 months

Showing 38013820 of 52,339 recalls

FoodNovember 29, 2024· The Kroger Co

Recalled Item: DELI FRESH VEGETABLE TRAY MED Recalled by The Kroger Co Due to Potential...

The Issue: Platters and trays prepared in-store may contain cut cucumbers that were...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 29, 2024· The Kroger Co

Recalled Item: BOAR'S HEAD HUMMUS VEG PLATTER MED Recalled by The Kroger Co Due to...

The Issue: Platters and trays prepared in-store may contain cut cucumbers that were...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 29, 2024· The Kroger Co

Recalled Item: SMALL VEGGIE PLATTER Recalled by The Kroger Co Due to Potential Salmonella...

The Issue: Platters and trays prepared in-store may contain cut cucumbers that were...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 29, 2024· BALOIAN FARMS

Recalled Item: whole fresh American cucumbers packaged in bulk cardboard containers labeled...

The Issue: Cucumbers potentially contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 27, 2024· Delta Fresh LLC.

Recalled Item: Product is a whole Recalled by Delta Fresh LLC. Due to Potential Salmonella...

The Issue: Potential Salmonella contamination of fresh cucumbers. Associated with an...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 27, 2024· AvKARE

Recalled Item: Cinacalcet Tablets Recalled by AvKARE Due to CGMP deviations: Presence of...

The Issue: CGMP deviations: Presence of Nitrosamine Drug Substance Related Impurity...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 27, 2024· AvKARE

Recalled Item: Cinacalcet Tablets Recalled by AvKARE Due to CGMP deviations: Presence of...

The Issue: CGMP deviations: Presence of Nitrosamine Drug Substance Related Impurity...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 27, 2024· AvKARE

Recalled Item: Cinacalcet Tablets Recalled by AvKARE Due to CGMP deviations: Presence of...

The Issue: CGMP deviations: Presence of Nitrosamine Drug Substance Related Impurity...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 27, 2024· IsoTis OrthoBiologics, Inc.

Recalled Item: OsteoSurge 100 Demineralized Bone Matrix Putty with Accell Bone Matrix...

The Issue: Incorrect expiration date listed on the outer box, which does not align with...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2024· IsoTis OrthoBiologics, Inc.

Recalled Item: OsteoCove Putty Recalled by IsoTis OrthoBiologics, Inc. Due to Hydration...

The Issue: Hydration issue resulting in the product being less cohesive and moldable...

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

Class II — Potential Health HazardOngoing
DrugNovember 26, 2024· Curium US, LLC

Recalled Item: Kit for the Preparation of Technetium Tc 99m Sestamibi Injection Recalled by...

The Issue: Lack of Assurance of Sterility; Improper crimps on vials impacting the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 26, 2024· O&M HALYARD, INC.

Recalled Item: Brand Name: HALYARD Product Name: Laparotomy Pack Model/Catalog Number:...

The Issue: Elevated residues of anti-block/slip additive used in manufacturing found...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2024· Beckman Coulter, Inc.

Recalled Item: Access Intact PTH assay Recalled by Beckman Coulter, Inc. Due to Beckman...

The Issue: Beckman Coulter has identified that some Access PTH reagent packs from lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2024· 3M Unitek Corporation

Recalled Item: 3M Unitek Transbond Plus Self-Etching Primer (100 unit Recalled by 3M Unitek...

The Issue: Due to an increase of complaints for bracket bond failures and skin...

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

Class II — Potential Health HazardOngoing
DrugNovember 25, 2024· Macleods Pharmaceuticals Ltd

Recalled Item: Olanzapine Tablets Recalled by Macleods Pharmaceuticals Ltd Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 25, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...

The Issue: The probe tips of the hand instruments are being damaged or breaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...

The Issue: The probe tips of the hand instruments are being damaged or breaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...

The Issue: The probe tips of the hand instruments are being damaged or breaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...

The Issue: The probe tips of the hand instruments are being damaged or breaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...

The Issue: The probe tips of the hand instruments are being damaged or breaking...

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

Class II — Potential Health HazardOngoing