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. 2,624 recalls have been distributed to Arizona in the last 12 months.
Showing 19221–19240 of 52,339 recalls
Recalled Item: ARTIS Pheno - Interventional Fluoroscopic X-Ray System Model: 10849000 -...
The Issue: If the C-arm leaves its intended travel path due to a fault within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pump Tube Set for MMS Libra and Solar Systems - Recalled by LABORIE MEDICAL...
The Issue: This field correction is being initiated to address potentially damaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioPlex 2200 Syphilis Total & RPR Linked Immunoabsorption Assay Recalled by...
The Issue: The increased level of RPR reactivity in the BioPlex 2200 Syphilis Total &...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus 235 The Proton Therapy System - Proteus 235 (brand Recalled by Ion...
The Issue: Signature from the user is necessary to proceed with specific actions in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart XL Monitor/Defibrillators Model number: M4735A - Product...
The Issue: HeartStart XL MonitorlDefibrillators may not have been included in prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infuvite PEDiatric Pharmacy Recalled by Sandoz, Inc Due to Defective...
The Issue: Defective Container: Sub-optimal crimping in vial of Pediatric Infuvite...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisinopril Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to Product...
The Issue: Product Mix-Up: a complaint received indicating mix-up of 10 mg Lisinopril...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ChapStick Total Hydration Moisture + Tint + SPF15 Very Berry Recalled by...
The Issue: Labeling: Not elsewhere classified: Observed separation in the secondary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketorolac Tromethamine Injection Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Presence of Particulate Matter - found in reserve sample vials at the firm.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ChapStick Total Hydration Moisture + Tint + SPF15 Peachy Keen Recalled by...
The Issue: Labeling: Not elsewhere classified: Observed separation in the secondary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketorolac Tromethamine Injection Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Presence of Particulate Matter - found in reserve sample vials at the firm.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ChapStick Total Hydration Moisture + Tint + SPF15 Pretty in Recalled by...
The Issue: Labeling: Not elsewhere classified: Observed separation in the secondary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5.5 oz cans of Ocean Spray Pink Lite Cranberry Juice Drink Recalled by Ocean...
The Issue: Product contains undeclared sulfites.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 14" Recalled by La Sonorense, Inc. Due to Undeclared Wheat
The Issue: The product does not properly display the list of ingredients and contains...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 16" Recalled by La Sonorense, Inc. Due to Undeclared Wheat
The Issue: The product does not properly display the list of ingredients and contains...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 12" Recalled by La Sonorense, Inc. Due to Undeclared Wheat
The Issue: The product does not properly display the list of ingredients and contains...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Siemens Cios Alpha VA30-mobile X-Ray system Recalled by Siemens Medical...
The Issue: Main cable can be plugged or unplugged from the X10 connector which is part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRUE METRIX SELF MONITORING BLOOD GLUCOSE SYSTEM - Product Usage: Recalled...
The Issue: One (1) TRUE METRIX AIR blood glucose meter distributed in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Regard. Item number: 830034. GS0348D- CVC Triple Lumen 20CM non Sulfa-Mercy....
The Issue: Custom procedure kits contains affected lots of PosiFlush Syringe, a product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Renuvion/ J-Plasma Precise Open Handpiece. Catalog numbers BVX-044-BPS...
The Issue: Unexpected stress fractures on the shaft of the hand piece may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.