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. 2,759 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,759 in last 12 months

Showing 70017020 of 52,339 recalls

DrugJanuary 16, 2024· Ascend Laboratories, LLC

Recalled Item: Fosfomycin Tromethamine Granules for Oral Solution Recalled by Ascend...

The Issue: Failed Impurities/Degradation Specification: Out of specification for...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 16, 2024· Den-Mat Holdings, LLC

Recalled Item: Hydrogen Peroxide Oral Rinse Recalled by Den-Mat Holdings, LLC Due to CGMP...

The Issue: CGMP Deviations: products may not conform to the labeled specifications.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 16, 2024· Den-Mat Holdings, LLC

Recalled Item: OralProCare medicated lip treatment Recalled by Den-Mat Holdings, LLC Due to...

The Issue: CGMP Deviations: products may not conform to the labeled specifications.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 16, 2024· Avanos Medical, Inc.

Recalled Item: MIC* Gastric-Jejunal Feeding Tube with ENFit Connectors: a) MIC*...

The Issue: MIC* Gastric - Jejunal Feeding Tube Kits contain a sterile pre-filled...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 16, 2024· Avanos Medical, Inc.

Recalled Item: MIC* Gastric-Jejunal Feeding Tube Recalled by Avanos Medical, Inc. Due to...

The Issue: MIC* Gastric - Jejunal Feeding Tube Kits contain a sterile pre-filled...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 16, 2024· W&H DENTALWERK BUERMOOS GMBH

Recalled Item: W&H Surgical handpiece S-12. For Surgical treatment of dental hard Recalled...

The Issue: 1:2 speed increasing surgical handpieces have been incorrectly laser marked...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2024· Maquet Medical Systems USA

Recalled Item: BEQ-HLS 7050 USA Recalled by Maquet Medical Systems USA Due to The Emergency...

The Issue: The Emergency Priming Line, a component of the HLS Set, may have a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2024· Maquet Medical Systems USA

Recalled Item: Model No. BEQ-HLS 5050 USA Recalled by Maquet Medical Systems USA Due to The...

The Issue: The Emergency Priming Line, a component of the HLS Set, may have a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2024· Olympus Corporation of the Americas

Recalled Item: Water Filter MAJ-2318. This MAJ-2318 water filter has been designed Recalled...

The Issue: Water filter may have been assembled incorrectly, resulting in unfiltered...

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

Class II — Potential Health HazardOngoing
DrugJanuary 15, 2024· Amneal Pharmaceuticals of New York, LLC

Recalled Item: Phenoxybenzamine Hydrochloride Capsules Recalled by Amneal Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 15, 2024· Medical Action Industries, Inc. 306

Recalled Item: IV Start Kit Recalled by Medical Action Industries, Inc. 306 Due to The kits...

The Issue: The kits contain saline flush syringes which were recalled by the supplier.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2024· D.O.R.C. Dutch Opthalmic Research Center Intl B.V.

Recalled Item: Directional Laser Probe with Alcon / Lumenis connector (27 gauge / 0.4 mm)...

The Issue: When using those products you may experience difficulties to extend or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2024· D.O.R.C. Dutch Opthalmic Research Center Intl B.V.

Recalled Item: Directional Laser Probe with Alcon / Lumenis connector (25 gauge / 0.5 mm)...

The Issue: When using those products you may experience difficulties to extend or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2024· D.O.R.C. Dutch Opthalmic Research Center Intl B.V.

Recalled Item: Directional Laser Probe with Alcon / Lumenis connector (23 gauge / 0.6 mm)...

The Issue: When using those products you may experience difficulties to extend or...

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

Class II — Potential Health HazardOngoing
DrugJanuary 12, 2024· Neptune Resources, LLC

Recalled Item: Neptune's Fix Recalled by Neptune Resources, LLC Due to Marketed without an...

The Issue: Marketed without an approved NDA/ANDA: Product contains tianeptine, a...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 12, 2024· Neptune Resources, LLC

Recalled Item: Neptune's Fix Recalled by Neptune Resources, LLC Due to Marketed without an...

The Issue: Marketed without an approved NDA/ANDA: Product contains tianeptine, a...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 12, 2024· Neptune Resources, LLC

Recalled Item: Neptune's Fix Recalled by Neptune Resources, LLC Due to Marketed without an...

The Issue: Marketed without an approved NDA/ANDA: Product contains tianeptine, a...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 11, 2024· Rizo Lopez Foods, Inc. dba Don Francisco Cheese

Recalled Item: 365 Whole Foods Market Ricotta Part Skim 15 oz. Recalled by Rizo Lopez...

The Issue: Listeria monocytogenes contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 11, 2024· Rizo Lopez Foods, Inc. dba Don Francisco Cheese

Recalled Item: Monterey Jack Conventional (bulk) Recalled by Rizo Lopez Foods, Inc. dba Don...

The Issue: Listeria monocytogenes contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 11, 2024· Rizo Lopez Foods, Inc. dba Don Francisco Cheese

Recalled Item: Tio Francisco Panela 14 oz. Food City Panela Recalled by Rizo Lopez Foods,...

The Issue: Listeria monocytogenes contamination.

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

Class I — Serious Health HazardOngoing
Refund