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. 2,802 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,802 in last 12 months

Showing 201220 of 52,339 recalls

FoodJanuary 9, 2026· Diva Fam Inc

Recalled Item: Sea Moss Gel Superfood Recalled by Diva Fam Inc Due to potential Clostridium...

The Issue: potential Clostridium botulinum contamination

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 9, 2026· Diva Fam Inc

Recalled Item: Sea Moss Gel Superfood Recalled by Diva Fam Inc Due to potential Clostridium...

The Issue: potential Clostridium botulinum contamination

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 9, 2026· Diva Fam Inc

Recalled Item: Sea Moss Gel Superfood Recalled by Diva Fam Inc Due to potential Clostridium...

The Issue: potential Clostridium botulinum contamination

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 9, 2026· Diva Fam Inc

Recalled Item: Sea Moss Gel Superfood Recalled by Diva Fam Inc Due to potential Clostridium...

The Issue: potential Clostridium botulinum contamination

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 9, 2026· Medartis AG

Recalled Item: Brand Name: APTUS Product Name: 2.5 TriLock Screw 16mm Recalled by Medartis...

The Issue: Mix up between specified lots of 2.5mm and 2.8mm outer diameter screws.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2026· Medartis AG

Recalled Item: Brand Name: APTUS Product Name: 2.8 TriLock Screw 16mm Recalled by Medartis...

The Issue: Mix up between specified lots of 2.5mm and 2.8mm outer diameter screws.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2026· FUJIFILM Healthcare Americas Corporation

Recalled Item: FDR Visionary Suite Recalled by FUJIFILM Healthcare Americas Corporation Due...

The Issue: It was found that the contacts of the electromagnetic contactors used inside...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2026· Maquet Cardiopulmonary Gmbh

Recalled Item: Bubble Sensor for 3/8" x 3/32" tubing Recalled by Maquet Cardiopulmonary...

The Issue: Internal investigations have identified an issue with the durability of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2026· Medline Industries, LP

Recalled Item: Medline Kits containing Tego Connectors Medline DIALYSIS ON/OFF KIT SKU...

The Issue: Affected lots may exhibit issues with the silicone seal on Tego Connectors...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2026· Medline Industries, LP

Recalled Item: Convenience kits containing Tego Connectors Medline DIALYSIS DRSNG CHNG SKU...

The Issue: Affected lots may exhibit issues with the silicone seal on Tego Connectors...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2026· Medline Industries, LP

Recalled Item: Convenience kits used for dialysis maintenance Medline ADD A CATH Recalled...

The Issue: Affected lots may exhibit issues with the silicone seal on Tego Connectors...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2026· Medline Industries, LP

Recalled Item: Medline Kits containing Tego Connectors: Medline IR Pack Recalled by Medline...

The Issue: Affected lots may exhibit issues with the silicone seal on Tego Connectors...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2026· Medline Industries, LP

Recalled Item: Convenience kits containing Tego Connectors: Medline DIALYSIS DRESSING...

The Issue: Affected lots may exhibit issues with the silicone seal on Tego Connectors...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2026· Medline Industries, LP

Recalled Item: Medline kits containing Tego Connectors Medline APHERESIS SUBQPORT ACCESS...

The Issue: Affected lots may exhibit issues with the silicone seal on Tego Connectors...

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

Class II — Potential Health HazardOngoing
FoodJanuary 7, 2026· Rich Products Corp

Recalled Item: GLUTEN FREE 14" SEASONED VEGAN PIZZA CRUST Recalled by Rich Products Corp...

The Issue: Product contains undeclared milk and egg

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 7, 2026· Medline Industries, LP

Recalled Item: Medline Convenience Kits: 1) KIT SURG ONC EXCISION BREAST Recalled by...

The Issue: Medline has identified issues related to calibration of the equipment used...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Medline Industries, LP

Recalled Item: Medline Convenience Kits: 1) KIT TRIPLE LUMEN INSERTION Recalled by Medline...

The Issue: Medline has identified issues related to calibration of the equipment used...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Medline Industries, LP

Recalled Item: Medline Convenience Kits: 1) KIT ACES INSERT PEG Recalled by Medline...

The Issue: Medline has identified issues related to calibration of the equipment used...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Medline Industries, LP

Recalled Item: Medline Convenience Kits: 1) DRAPE PACK-CHOICE Recalled by Medline...

The Issue: Medline has identified issues related to calibration of the equipment used...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2026· Medline Industries, LP

Recalled Item: Medline Convenience Kits: 1) LVAD DRIVELINE TRAY Recalled by Medline...

The Issue: Medline has identified issues related to calibration of the equipment used...

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

Class II — Potential Health HazardOngoing