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. 2,725 recalls have been distributed to Arizona in the last 12 months.
Showing 12881–12900 of 29,154 recalls
Recalled Item: PneumoDart Recalled by Tytek Medical Inc Due to A defect involving an...
The Issue: A defect involving an occluded needle was discovered during a training exercise.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-PACK B12 Pretreatment Set- IVD for diagnostic use for pre-treatment...
The Issue: The AIA-2000 bar code scanners depend on the quiet zone to help identify the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Berman Angiographic Catheter 60cm Item Number: AI-07130-J Recalled by...
The Issue: Potential leak in the balloon extension line. If a leak was present and went...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Berman Angiographic Catheter 50cc Item Number: AI-07130 Recalled by...
The Issue: Potential leak in the balloon extension line. If a leak was present and went...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HardyCHROM MRSA Recalled by Hardy Diagnostics Due to False Positive results...
The Issue: False Positive results due to the MSSA (methicillin-susceptible) strain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis Precise Nitinol Stent System. The Cordis PRECISE Nitinol Stent...
The Issue: Cordis has initiated a labeling correction for S.M.A.R.T. and PRECISE stents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S.M.A.R.T. Nitinol Stent System and the S.M.A.R.T. Control Nitinol Stent...
The Issue: Cordis has initiated a labeling correction for S.M.A.R.T. and PRECISE stents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis S.M.A.R.T. CONTROL /S.M.A.R.T. Vascular Stent System. The S.M.A.R.T....
The Issue: Cordis has initiated a labeling correction for S.M.A.R.T. and PRECISE stents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eleganza 5 (AC powered adjustable bed) Recalled by Linet Spol. S.r.o. Due to...
The Issue: A component used within the side rail mechanism may malfunction, resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Cardiopulmonary GmbH / Getinge Quadrox-iD Pediatric Diffusion...
The Issue: Sterile barrier system may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENDURO SPECIAL KEY TIB.LOCK.RING F1/10MM product code NP462R used with...
The Issue: Nonfunctional key due to the potential for damage to the key pins cause by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stratum MDS Screw 3.5x50mm ST Part Number: STRM-MDS-3550ST Recalled by...
The Issue: Components 2mm shorter than indicated on the package label
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stratum MDS Screw 3.5x46mm ST Part Number: STRM-MDS-3546ST Recalled by...
The Issue: Components 2mm shorter than indicated on the package label
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stratum MDS Screw 3.5x48mm ST Part Number: STRM-MDS-3548ST Recalled by...
The Issue: Components 2mm shorter than indicated on the package label
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLASSIC Radiofrequency Cannula - Curved Recalled by Abbott Medical Due to A...
The Issue: A manufacturing error caused a single lot of 10mm active tip length Cannulas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smith&nephew PROFIX Mallet Recalled by Smith & Nephew, Inc. Due to There is...
The Issue: There is a a potential failure mode associated with the use of the mallet,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioJet Ultra Consoles-Thrombectomy System UPN: 105650-001D 105650-001H...
The Issue: Missing Directions for Use (DFU) - Consoles shipped to customers without the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iChem VELOCITY Urine Chemistry Analyzer Recalled by Beckman Coulter Inc. Due...
The Issue: Beckman Coulter has become aware of an issue affecting Specific Gravity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ligamax 5 mm Endoscopic Multiple Clip Applier Recalled by Ethicon...
The Issue: A potential exists that certain LIGAMAX devices within the impacted lots may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cognision Recalled by Neuronetrix Solutions, LLC dba Cognision Due to...
The Issue: Product has the potential to be contaminated with Burkholderia cepacia (B....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.