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.
Showing 7921–7940 of 29,154 recalls
Recalled Item: Medicina Reusable Oral syringe 2.5ml Code: OTH25 Recalled by Medicina Uk Ltd...
The Issue: Plunger component has been manufactured with an unapproved material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medicina Reusable Oral syringe 1ml Code: OTH01 Recalled by Medicina Uk Ltd...
The Issue: Plunger component has been manufactured with an unapproved material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Da Vinci S/Si Large Clip Applier Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Due to the potential for unexpected motion caused by the partial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Da Vinci X/Xi Large Clip Applier Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Due to the potential for unexpected motion caused by the partial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Echelon -14 Recalled by Micro Therapeutics, Inc. Due to Outer carton...
The Issue: Outer carton packaging of microcatheters were exposed to wet substance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Echelon -14 Micro Catheter Recalled by Micro Therapeutics, Inc. Due to Outer...
The Issue: Outer carton packaging of microcatheters were exposed to wet substance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthex External Fixation Wire Sharp Bayonet 1.8 x 400 mm Model: K400-18BN...
The Issue: Manufacturing variance near transition of tip is increasing the likelihood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARTO VIZIGO 8.5F Bi-Directional Guiding Sheath Recalled by Biosense...
The Issue: Outside packaging for a device indicated for introducing cardiovascular...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sklar Instruments IV Cath Dressing Tray Cs/25 Re-Order Number: 96-1708...
The Issue: Kits mislabeled as latex-free, the packaging for component 94-7002...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wolf Pak Premium Dressing Change Kit with GuardVA and Statlok Recalled by...
The Issue: Kits mislabeled as latex-free, the packaging for component 94-7002...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wolf Pak Premium Dressing Change Kit with Statlock CS/30 Recalled by Trinity...
The Issue: Kits mislabeled as latex-free, the packaging for component 94-7002...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wolf-Pak Premium Dressing Kit with GuardVA Cs/30 Recalled by Trinity...
The Issue: Kits mislabeled as latex-free, the packaging for component 94-7002...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE MICRO-KILL GERMICIDAL BLEACH WIPES Recalled by MEDLINE INDUSTRIES,...
The Issue: stability failure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE Measured Sizing and Rotation Guide-to size the femur and Recalled by...
The Issue: Manufactured with a Galvanized High Carbon Steel spring instead of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SX-One MicroKnife Recalled by SONEX HEALTH LLC Due to Potential of dull blade
The Issue: Potential of dull blade
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist Device (HVAD) System Batteries Recalled by...
The Issue: Battery performance issues. Battery electrical faults render it unable to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Iron_2 (Iron_2) is for in vitro diagnostic use Recalled by...
The Issue: Falsely Elevated Atellica CH Microalbumin_2 (¿ALB_2) Results due to Reagent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Description/Item: ChemoLock Bag Spike Recalled by ICU Medical, Inc....
The Issue: Ports have a potential for unintended disconnection, inability to connect to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Description/Item: ChemoLock Vial Spike Recalled by ICU Medical, Inc....
The Issue: Ports have a potential for unintended disconnection, inability to connect to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HAMILTON-C6 Intensive Care Ventilator Recalled by Hamilton Medical AG Due to...
The Issue: Ventilator status indicator board can become loose, which could lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.