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. 2,778 recalls have been distributed to Arizona in the last 12 months.
Showing 4541–4560 of 29,154 recalls
Recalled Item: Dilator - Intended to be used for dilating puncture sites Recalled by Cook...
The Issue: Packaging may have low seal strength and not meet peel strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Entuit Secure Adjustable Gastrointestinal Suture Anchor Set - Intended for...
The Issue: Packaging may have low seal strength and not meet peel strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Yueh Centesis Disposable Catheter Needle - Intended for use in Recalled by...
The Issue: Packaging may have low seal strength and not meet peel strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trocar Needle - Used for dilating puncture sites or catheter Recalled by...
The Issue: Packaging may have low seal strength and not meet peel strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dilator - Coons Taper - Used for dilating puncture sites Recalled by Cook...
The Issue: Packaging may have low seal strength and not meet peel strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dilator With AQ Hydrophilic Coating - Intended to be used Recalled by Cook...
The Issue: Packaging may have low seal strength and not meet peel strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mojo 2 Full Face AAV Non Vented Mask Recalled by SleepNet Corporation Due to...
The Issue: Update to contraindications and warning language due to CPAP masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iQ 2 Nasal Vented Mask Recalled by SleepNet Corporation Due to Update to...
The Issue: Update to contraindications and warning language due to CPAP masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mojo 2 Full Face Non Vented Mask Recalled by SleepNet Corporation Due to...
The Issue: Update to contraindications and warning language due to CPAP masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mojo Non Vented Full Face Mask with Headgear Recalled by SleepNet...
The Issue: Update to contraindications and warning language due to CPAP masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mojo 2 Full Face Vented Mask Recalled by SleepNet Corporation Due to Update...
The Issue: Update to contraindications and warning language due to CPAP masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phantom 2 Nasal Vented Mask Recalled by SleepNet Corporation Due to Update...
The Issue: Update to contraindications and warning language due to CPAP masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mojo Full Face with Headgear Recalled by SleepNet Corporation Due to Update...
The Issue: Update to contraindications and warning language due to CPAP masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Cholestech LDX Battery Kit Recalled by Alere San Diego, Inc. Due to...
The Issue: There is a potential that the Cholestech LDX battery (an external battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure kits Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Trumpet Needle Guide ring can detach when excessive pressure is applied.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion OB INSTRUMENT TRAY Recalled by MEDLINE INDUSTRIES, LP - Northfield...
The Issue: Trumpet Needle Guide ring can detach when excessive pressure is applied.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: N-LHP-928 Recalled by PACIFIC LASERTECH, LLC Due to These laser products...
The Issue: These laser products fail to comply with 21 CFR 1040.10(f)(4) Key control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 25-LHP-928 Recalled by PACIFIC LASERTECH, LLC Due to These laser products...
The Issue: These laser products fail to comply with 21 CFR 1040.10(f)(4) Key control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 25-LHP-828 Recalled by PACIFIC LASERTECH, LLC Due to These laser products...
The Issue: These laser products fail to comply with 21 CFR 1040.10(f)(4) Key control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Triangle Tip Electrosurgical Knives- to be used with Olympus...
The Issue: Due to increase in complaints for the KD-640L and KD-645L Triangle Tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.