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. 2,764 recalls have been distributed to Arizona in the last 12 months.
Showing 6681–6700 of 29,154 recalls
Recalled Item: GEO Instrument Kit for EPS Plate Recalled by GRAMERCY EXTREMITY ORTHOPEDICS...
The Issue: Instrument Kits for EPS plates may contain drill guides with incorrect drill...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pilot COVID-19 At-Home Test Recalled by SD Biosensor, Inc. Due to The liquid...
The Issue: The liquid buffer component in the affected test kit lots was determined to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: greiner bio-one VACUETTE TUBE 6 ml K3E K3EDTA Recalled by Greiner Bio-One...
The Issue: Some of the tubes may be incorrectly labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom pro+ mattress Recalled by Baxter Healthcare Corporation Due to...
The Issue: There is a potential for mattress cover damage (delamination) which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eye and Ear Dropper Recalled by Apothecary Products, LLC Due to Potential...
The Issue: Potential for glass dropper to have glass particulate on the outside surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medicine Dropper Recalled by Apothecary Products, LLC Due to Potential for...
The Issue: Potential for glass dropper to have glass particulate on the outside surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DYND3000xxP Series - Flexible Laryngeal Mask Airway Packs Recalled by...
The Issue: The case and each (i.e. packet) labels for the DYND3000xxP series do not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Immundiagnostik IDK Lactoferrin ELISA- In vitro enzyme immunoassay intended...
The Issue: Marketed without a 510k
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TDHisto/Cyto - A software product used for managing medical information...
The Issue: In a specific use case, when printing labels for slides, some labels may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM NEUROTUBE Recalled by Baxter Healthcare Corporation Due to The product...
The Issue: The product is brittle and potentially crumbling upon handling or when being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JOURNEY II UNI XLPE TIBIA INSERT MEDIAL SZ 7-8 8MM Recalled by Smith &...
The Issue: A mispack occurred during the manufacturing process, resulting in the box...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEX. BIOPSY FORCEPS 5FR WL 550MM Recalled by Richard Wolf GmbH Due to...
The Issue: Potentially unable to open forceps jaws when the endoscope shaft is bent by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEX. GRASP. FORCEPS 5FR WL 550MM Recalled by Richard Wolf GmbH Due to...
The Issue: Potentially unable to open forceps jaws when the endoscope shaft is bent by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEX. GRASP. FORCEPS 6.6FR WL 550MM Recalled by Richard Wolf GmbH Due to...
The Issue: Potentially unable to open forceps jaws when the endoscope shaft is bent by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEX. GRASP. FORCEPS 5FR WL 550MM Recalled by Richard Wolf GmbH Due to...
The Issue: Potentially unable to open forceps jaws when the endoscope shaft is bent by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shiley Adult Flexible Tracheostomy Tube with TaperGuard Cuff Recalled by...
The Issue: A manufacturing error, resulted in a less than specified diameter of adult...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WALGREENS BANDAGES Recalled by ASO LLC Due to The adhesive bandage contains...
The Issue: The adhesive bandage contains 0.1% benzalkonium chloride impregnated in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA Compact Automated Multi-Parametric Analyzer Recalled by Diagnostica...
The Issue: An internal investigation identified a bug in this firmware version,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA Compact Max fully automatic clinical analyzer Recalled by Diagnostica...
The Issue: An internal investigation identified a bug in this firmware version,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA R Max fully automatic clinical instrument designed to perform Recalled...
The Issue: An internal investigation identified a bug in this firmware version,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.