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. 1,096 recalls have been distributed to Arizona in the last 12 months.
Showing 12741–12760 of 29,154 recalls
Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 12MM STERILE Recalled by Synthes, Inc....
The Issue: There is a possibility that the inner cap could open when the outer cap is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microbiologics QC Sets and Panels Recalled by Microbiologics Inc Due to The...
The Issue: The recommended hydration fluid for the 8180 Gram-Positive Blood Culture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Universal Viewer 6.0 Recalled by GE Healthcare, LLC Due to...
The Issue: Centricity Universal Viewer measurements saved into a DICOM Grayscale...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 18MM STERILE Recalled by Synthes, Inc....
The Issue: There is a possibility that the inner cap could open when the outer cap is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 10MM STERILE Recalled by Synthes, Inc....
The Issue: There is a possibility that the inner cap could open when the outer cap is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 24MM STERILE Recalled by Synthes, Inc....
The Issue: There is a possibility that the inner cap could open when the outer cap is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 16MM STERILE Recalled by Synthes, Inc....
The Issue: There is a possibility that the inner cap could open when the outer cap is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HUDSON RCI COMFORT FLO Humidification System Recalled by TELEFLEX MEDICAL...
The Issue: There is the potential for water to flood the column and enter the circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HUDSON RCI COMFORT FLO Corrugated Humidification System Recalled by TELEFLEX...
The Issue: There is the potential for water to flood the column and enter the circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter MicroScan PROMPT Inoculation System-D Recalled by Beckman...
The Issue: Due to customer reports it has been determined that the inoculation system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HUDSON RCI COMFORT FLO Humidification System With Remote Temperature Port...
The Issue: There is the potential for water to flood the column and enter the circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HUDSON RCI COMFORT FLO Corrugated Humidification System with Remote...
The Issue: There is the potential for water to flood the column and enter the circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANCED ENDOSEE System CANNULA Recalled by CooperSurgical, Inc. Due to...
The Issue: Potential for unsealed pouches in two (2) lots of the Endosee Advance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clearlink System Continu-Flo Administration Sets Recalled by Baxter...
The Issue: Continu-Flo sets with male Luer bodies at the lower end of, and within, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ONE-LINK Needle-free IV Connector Recalled by Baxter Healthcare Corporation...
The Issue: Continu-Flo sets with male Luer bodies at the lower end of, and within, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion- Dressing Tray M101156A DRESSING TRAY M101167A DRESSING TRAY...
The Issue: Incomplete seals on the sterile package may compromise the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brasseler USA KM169-39-76 Steinmann Pin Single Diamond Smooth Recalled by...
The Issue: 103 packaged and labeled tubes (103 product tubes with 6 pins per tube) of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion-LVAD Kits DM1005 DAILY LVAD MAINTENANCE KIT DM280A LVAD MANAGEMENT...
The Issue: Incomplete seals on the sterile package may compromise the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion- Pelvic Exam Kits DYNDE1037 PELVIC EXAM TRAY Recalled by Centurion...
The Issue: Incomplete seals on the sterile package may compromise the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion- SPEC0002B ARTHROGRAM TRAY SPEC0002B ARTHROGRAM TRAY SPEC0004C...
The Issue: Incomplete seals on the sterile package may compromise the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.