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. 2,798 recalls have been distributed to Arizona in the last 12 months.
Showing 2341–2360 of 29,154 recalls
Recalled Item: CircuitGuard ThermoFlo Filter -Combined Heat and Moisture Exchanger Recalled...
The Issue: The machine side connector of the filter HME may be occluded by plastic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 138913-01 BD PYXIS MEDBANK MINI CR-2HH-1FH-P 169-114 BD PYXIS MEDBANK...
The Issue: Labeling update to include a contraindication statement against the use of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 139054-01 BD PYXIS MEDFLEX MN 1000 10HH-1FM 139055-01 BD PYXIS Recalled by...
The Issue: Labeling update to include a contraindication statement against the use of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 155288-01 BD PYXIS MEDBANK MINI 1FH-1FM 169-137 BD PYXIS MEDBANK Recalled by...
The Issue: Labeling update to include a contraindication statement against the use of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 139088-01 BD PYXIS MEDBANK MEDPASS MODULE 169-151 BD PYXIS MEDBANK Recalled...
The Issue: Labeling update to include a contraindication statement against the use of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Pyxis MedStation ES Recalled by CareFusion 303, Inc. Due to Software...
The Issue: Software issues could potentially result in: 1) delays in accessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The MSOT Acuity Echo is a Class 4 medical laser Recalled by Ithera Medical...
The Issue: The MSOT Acuity Echo does not include an adequate instruction for safe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) BD Pyxis MedStation ES Recalled by CareFusion 303, Inc. Due to Labeling...
The Issue: Labeling is insufficient regarding delays in access to medication. The firm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Rapid fFN Specimen Collection Tube (PN: 71550-001) is a Recalled by...
The Issue: Three lots of Rapid fFN Specimen Collection kit (901164, 901165, and 904850)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sysmex PS-10 Sample Preparation System with software version 1.5 and 1.6....
The Issue: Sysmex was made aware of a report of false results due to carry-over caused...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen LCCK Legacy Articular Surface with Locking Screw - Striped Yellow/E...
The Issue: It was identified internally that two commingle events occurred where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen LCCK Legacy Articular Surface with Locking Screw - Striped Purple/C...
The Issue: It was identified internally that two commingle events occurred where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Irix-A Integrated Lumbar Fusion System Recalled by XTANT Medical Holdings,...
The Issue: Certain implants in the Irix-A Lumbar Fusion System were distributed while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: SenTiva" Product Name: VNS Therapy" SenTiva" Recalled by...
The Issue: Their is a potential that implanted pulse generators may stop delivering...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: SenTiva DUO" Product Name: VNS Therapy¿ SenTiva DUO" Recalled by...
The Issue: Their is a potential that implanted pulse generators may stop delivering...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Socrates 38 Aspiration Catheter 127 cm length The Recalled by Scientia...
The Issue: Due to manufacturing non-conformance that resulted in channels in the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brasseler ESR Rotary/Reciprocating Endodontic File Device SKU AP120213PK...
The Issue: Due to devices being irradiated above the established specification which my...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access PCT Reagent Pack Recalled by Beckman Coulter Inc. Due to Identified...
The Issue: Identified reagent lots are experiencing a high rate of calibration failures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Belmont Medical 3-Spike Disposable Set used with the Belmont Rapid Recalled...
The Issue: Disposable set may leak during priming from a female quick connector due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline General Surgery Tray kits: 1) ARTERIAL LINE TRAY Recalled by MEDLINE...
The Issue: The catheter subassembly in the Integrated Arterial Catheter was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.