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 52,339 recalls
Recalled Item: Halyard CPT PEDS ADULT CH PACK - Medical convenience kits Recalled by AVID...
The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard LINE INSERTION PACK - Medical convenience kits Model Number:...
The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard MINOR PDS - Medical convenience kits Model Number: GVVA009-06...
The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard SAMMC-N PACEMAKER - Medical convenience kits Model Number:...
The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chameleon PTA Balloon Catheter with Injection Port 5mm x 40mm Recalled by...
The Issue: Specific lots of the Chameleon PTA Balloon Catheter failed to meet in-house...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AD-TECH Spencer Probe Depth Electrode Recalled by Ad-Tech Medical Instrument...
The Issue: Ad-Tech is recalling these A-Style SD Depth Electrodes because a label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AD-TECH Spencer Probe Depth Electrode Recalled by Ad-Tech Medical Instrument...
The Issue: Ad-Tech is recalling these A-Style SD Depth Electrodes because a label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AD-TECH Spencer Probe Depth Electrode Recalled by Ad-Tech Medical Instrument...
The Issue: Ad-Tech is recalling these A-Style SD Depth Electrodes because a label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Veklury (remdesivir) for injection Recalled by Gilead Sciences, Inc. Due to...
The Issue: Presence of Particulate Matter: Presence of glass particle.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medtronic Recharger Kits Recalled by Medtronic Neuromodulation Due to The...
The Issue: The Wireless Rechargers in the kits may be unable to enter a recharging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nihon Kohden Adult/Pediatric Forehead Disposable SpO2 Sensor Recalled by...
The Issue: Due to oximeters not having FDA market approval or clearance to distribute...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A1CNow+ Multi-Test HbA1c System consists of (1) a semi-disposable...
The Issue: The reason for this recall is PTS Diagnostics, Inc. received complaints of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: a. Hillrom Centrella Smart+ Medical-Surgical Hospital Bed Recalled by Baxter...
The Issue: The beds have a potential for an interface issue with the Rauland Responder...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nihon Kohden Adult Ear Clip SpO2 Sensor Recalled by Nihon Kohden America Inc...
The Issue: Due to oximeters not having FDA market approval or clearance to distribute...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190 Product...
The Issue: To better define the drying procedures described in the IFU to improve the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The IMAGEnet 6 Ophthalmic Data System is a software program Recalled by...
The Issue: The overlay of visual field test locations on a probability map, as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cartesion Prime Recalled by Canon Medical System, USA, INC. Due to When...
The Issue: When PET-CT system is executing reconstruction, if PET acquisition for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantimetrix Urine Chemistry Control Set Dipper Urinalysis Dipstick Testing...
The Issue: The Quantimetrix Dipper Urinalysis Dipstick control was shipped without the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Saphena Medical Venapax XL- Endoscopic Vessel Harvesting System for use...
The Issue: A Gen 5 tail piece was assembled to a Gen 4 Finished Device, resulting in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atovaquone Oral Suspension Recalled by Bionpharma Inc. Due to Microbial...
The Issue: Microbial Contamination of a Non-sterile Product: The product was found to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.