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. 1,978 recalls have been distributed to Arizona in the last 12 months.
Showing 16461–16480 of 29,154 recalls
Recalled Item: BOX PST03699 KIT APP MED ALTERNATIV STAP Product Usage: The Recalled by...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SLEEVEGK1 ZESTAW DO ZABIEGOW SLEEVEX1 Product Usage: The Endo GIA Recalled...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOX KIT00713 KIT BY PASS Product Usage: The Endo GIA Recalled by COVIDIEN...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) BOX LAPZD ZESTAW DO SG (2) BOX LAPISG1 ZESTAW Recalled by COVIDIEN...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1)BOX HEMIGX1 ZESTAW DO HEMICOLECTOMII (Item Number HEMIGX1 ZESTAW DO...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOX TGGLOGOWX1 DO TOTAL GASTRECTOMIII Product Usage: The Endo GIA Recalled...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA" Auto Suture" Universal Articulating Loading Unit 30mm - Recalled...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOX1073076GASB1 BBR GASTRIC BYPASS S(Item Code BOX1073076GASB1 BBR GASTRIC...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABX Pentra Micro ALBUMIN 2 CP Recalled by Horiba Instruments, Inc dba Horiba...
The Issue: When the ABX Pentra Micro ALBUMIN 2 CP (ALBT2) Reagent 2 is sampled and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convatec Esteem(TM) Synergy Stomahesive(R) Recalled by ConvaTec, Inc Due to...
The Issue: It was discovered that the stoma hole of one lots of the Esteem synergy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE Sterile* Needle Counter Recalled by Medline Industries Inc Due to...
The Issue: The product packaging seal has the potential to experience seal creep. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE Sterile* Needle Counter Recalled by Medline Industries Inc Due to...
The Issue: The product packaging seal has the potential to experience seal creep. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE O.R. Necessities(TM) Sterile* Needle Counter Recalled by Medline...
The Issue: The product packaging seal has the potential to experience seal creep. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE O.R. Necessities(TM) Sterile* Needle Counter Recalled by Medline...
The Issue: The product packaging seal has the potential to experience seal creep. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE O.R. Necessities(R) STERILE R Recalled by Medline Industries Inc Due...
The Issue: The product packaging seal has the potential to experience seal creep. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE Sterile* Needle Counter Recalled by Medline Industries Inc Due to...
The Issue: The product packaging seal has the potential to experience seal creep. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: t:slim G4 Insulin Pump with Dexcom G4 Platinum CGM Software version: 4.3.4.3...
The Issue: The fuel gauge, the component that reads and reports the battery parameters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Go.Up Recalled by Siemens Medical Solutions USA, Inc Due to There is...
The Issue: There is a potential for a software issue that may cause the need for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINX Management System Recalled by Torax Medical, Inc. Due to Possible out...
The Issue: Possible out of specification condition which may allow a bead component to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINX Management System Recalled by Torax Medical, Inc. Due to Possible out...
The Issue: Possible out of specification condition which may allow a bead component to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.