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. 1,071 recalls have been distributed to Arizona in the last 12 months.
Showing 16961–16980 of 52,339 recalls
Recalled Item: ACIST Kodama Intravascular Ultrasound Catheter The Kodama Intravascular...
The Issue: Test results from the manufacturing line found a piece of damaged o-ring in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiation therapy software Recalled by RaySearch America Inc Due to A...
The Issue: A software bug affecting results when using deep learning (DL) segmentation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oseltamivir Phosphate for Oral Suspension Recalled by Lupin Pharmaceuticals...
The Issue: Failed Impurities/Degradation Specifications; Out-of-specification test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine/Tetracaine (LIPO110)* 23%/7% Ointment 100 GMS per 4 ounce plastic...
The Issue: Superpotent Drug. Lidocaine higher concentration than listed
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Milex Gellhorn Flexible under the following labels: 1) Gellhorn Flexible...
The Issue: The affected Milex Gellhorn pessaries were incorrectly manufactured with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OT1000 Series Orthopedic Surgical Tables Recalled by Steris Corporation Due...
The Issue: On January 7, 2021, STERIS identified that the glued bond between the beam...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Band Recalled by G & H Wire Company Due to The text on the patient pack is...
The Issue: The text on the patient pack is correct and the product itself remains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Door County Coffee & Tea Co. French Vanilla Flavored Cappuccino. Recalled by...
The Issue: Retail Box did not contain list of ingredients or allergen statement.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Stryker Sustainability Solutions Ethicon Endo-Surgery Recalled by Stryker...
The Issue: Product was distributed without receiving regulatory clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various reprocessed products: PROVISION Recalled by ReNovo, Inc. Due to...
The Issue: Non-sterile product was shipped to customers labelled as sterile.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captivator/Captiflex/Sensation Short Throw Single-Use Polypectomy Snares...
The Issue: Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captivator Single-Use Polypectomy Snares Recalled by Boston Scientific...
The Issue: Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AntIbody to SARS-CoV-2 - Product Usage: (Colloidal Gold) for IgG/IgM...
The Issue: Distributed COVID test kits without emergency use authorization.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captivator II Single-Use Polypectomy Snares Outer box UPN Recalled by Boston...
The Issue: Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tube Tracheostomy and Tube Cuff Recalled by Smiths Medical ASD Inc. Due to...
The Issue: Smiths Medical became aware that three lot numbers of a specific model of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...
The Issue: Locking mechanism has been observed to disassociate either intraoperatively...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...
The Issue: Locking mechanism has been observed to disassociate either intraoperatively...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...
The Issue: Locking mechanism has been observed to disassociate either intraoperatively...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SARS-CoV-2 Antigen Test Recalled by Qiagen Sciences LLC Due to QIAGEN has...
The Issue: QIAGEN has become aware of the potential for false positive results to occur...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...
The Issue: Locking mechanism has been observed to disassociate either intraoperatively...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.