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. 2,582 recalls have been distributed to Arizona in the last 12 months.
Showing 20601–20620 of 52,339 recalls
Recalled Item: fentaNYL 500 mcg/250 mL (2 mcg/mL) Bupivacaine HCl 0.1% 250 Recalled by QuVa...
The Issue: Presence of Particulate matter: manufacturer recalled fentanyl API due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL 200 mcg/100 mL (2 mcg/mL) 0.125% Bupivacaine HCl 125 Recalled by...
The Issue: Presence of Particulate matter: manufacturer recalled fentanyl API due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL 400 mcg/200 mL (2 mcg/mL) ROPivacaine HCl 0.2% 400 Recalled by QuVa...
The Issue: Presence of Particulate matter: manufacturer recalled fentanyl API due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Albuterol 1.25mg / Ipratropium 0.5mg/ Budesonide 0.25mg Recalled by...
The Issue: Lack of Processing Controls
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amiodarone Hydrochloride Injection Recalled by AuroMedics Pharma LLC Due to...
The Issue: Crystallization: Presence of visible particulate matter.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amiodarone Hydrochloride Injection Recalled by AuroMedics Pharma LLC Due to...
The Issue: Crystallization: Presence of visible particulate matter.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amiodarone Hydrochloride Injection Recalled by AuroMedics Pharma LLC Due to...
The Issue: Crystallization: Presence of visible particulate matter.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine HCl Injection Recalled by AuroMedics Pharma LLC Due to Foreign...
The Issue: Presence of Foreign Substance: Foreign material found inside the vial.
Recommended Action: Stop taking this medication. Contact your pharmacy or 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: 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: 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: 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: 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: Marketside Creamy Cauliflower Parmesan Soup 16 ounce Codes: 8113130606...
The Issue: Soup labeled Creamy Cauliflower Parmesan Soup may contain undeclared fish...
Recommended Action: Do not consume. Return to store for a refund or discard.
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: Bow & Arrow Recalled by Med Man Distribution, Inc. Due to Undeclared Sildenafil
The Issue: Marketed without an Approved NDA/ANDA: Product contains undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Natrum Sulphuricum 6X Tablets Recalled by Washington Homeopathic Products,...
The Issue: CGMP Deviations: products were not manufactured under current good...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pareira (Brava) 1X Tincture Recalled by Washington Homeopathic Products,...
The Issue: CGMP Deviations: products were not manufactured under current good...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Natrum Phosphoricum 6X Tablets Recalled by Washington Homeopathic Products,...
The Issue: CGMP Deviations: products were not manufactured under current good...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Calcarea Sulphurica 6X Tablets Recalled by Washington Homeopathic Products,...
The Issue: CGMP Deviations: products were not manufactured under current good...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.