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. 2,782 recalls have been distributed to Arizona in the last 12 months.
Showing 3901–3920 of 29,154 recalls
Recalled Item: KNEE ARTHROSCOPY PACK-Procedure Kit Catalog Number: WEKA15B Recalled by...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL Recalled by American Contract Systems Inc Due to Ethylene Oxide/Ethylene...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HAND PACK 297829--Procedure Kit Catalog Number: RGHN04I Recalled by American...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KNEE ARTHROSCOPY PACK-Procedure Kit Catalog Number: SFAR60A Recalled by...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventilator HAMILTON-C6 Recalled by Hamilton Medical AG Due to Ventilator may...
The Issue: Ventilator may enter sensor fail mode, ventilation may not re-initiate,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUETTE¿ TUBE 8 ml CAT Serum Separator Clot Activator 16x100 Recalled by...
The Issue: The firm received reports that some blood collection tubes have experienced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Calibrator Kit 29- In-Vitor used to calibrate...
The Issue: Kit assigned an extended expiration date of 24-Jul-2025 during release. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMT Initial Placement Dilator Set. Used to place gastrostomy devices....
The Issue: Devices were labelled with the incorrect guidewire labelling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage PureFlow-B Solution Recalled by NxStage Medical Inc Due to The...
The Issue: The smaller chamber of the two chamber bag is bursting when nurses are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-sterile Recalled by SVS LLC Due to Mislabeling
The Issue: Firm received complaints regarding skin irritation when using the gloves,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis Recalled by CareFusion 303, Inc. Due to Multiple socket-outlet...
The Issue: Multiple socket-outlet power strips that shipped with automated dispensing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis Recalled by CareFusion 303, Inc. Due to Multiple socket-outlet...
The Issue: Multiple socket-outlet power strips that shipped with automated dispensing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aeos Robotic Digital Microscope Recalled by Aesculap Inc Due to Possibility...
The Issue: Possibility of the robotic arm to drop more than 10cm from its original...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sight OLO CBC Test Kit Recalled by SIGHT DIAGNOSTICS LTD Due to One Test Kit...
The Issue: One Test Kit lot (TK1-10114) shows a positive bias in the platelet count due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity Acute Care System (IACS) Monitoring System Recalled by Draeger...
The Issue: Device is not in full compliance to Type CF requirements of IEC 60601-1 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu-Chek Guide (SC) Kit -Intended to quantitatively measure glucose in...
The Issue: The reason for recall is the meters may show an incorrect measurement unit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Darby Prophylaxis Paste with 1.23% Fluoride Ion Recalled by Young Dental...
The Issue: Part number 040032, Lot number, 248607 was incorrectly labeled as part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica HistoCore Arcadia H Recalled by LEICA BIOSYSTEMS NUSSLOCH GMBH Due to...
The Issue: An issue with safe usage of the device was identified whereby toxic smoke...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Ascenda Intrathecal Catheter Recalled by Medtronic Neuromodulation...
The Issue: Design update to the Ascenda Intrathecal Catheter Models 8780, 8781, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MRI systems: Vantage Orian MRT-1550 (MEXL-1550) Recalled by Canon Medical...
The Issue: The terminal block used to secure the power supply cable for the gradient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.