Recalls distributed in Arizona
These notices name Arizona in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.
3,983 stored notices name Arizona, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Arizona too — those are in the archive.
Reported Oct 12, 2022
Philips Respironics Amara View Minimal Contact Full-Face Mask
High riskUsing this product could cause serious injury, illness or death — stop using it now.Philips Respironics, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 5, 2022
BD Pyxis MedBank Cabinet Software v2.1.2.9 Legacy MedBank Cabinets with Matrix Drawers include: . CUBEX MedFlex…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Oct 5, 2022
Humidifier bottle and syringe filter kit (6 count of each) for the BT37 Mark I Benchtop Incubator (AY102295). The Mark…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 5, 2022
MEDLINE CLEARPRO DOUBLE SWIVEL CLOSED SUCTION CATHETER, flat peel pouch EA, 10 EA per Inner Carton (IC), 20 EA/2 Inner…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MEDLINE INDUSTRIES, LP - Northfield
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 5, 2022
OSSUR Power Knee REF PKA10003 OSSUR Power Knee REF PKA10003 OSSUR Power Knee REF PKA01001L OSSUR Power Knee REF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ossur Americas
FDA (openFDA device enforcement)
Reported Oct 5, 2022
t:slim X2 insulin pump; t:slim X2 insulin pump with Dexcom G5; t:slim X2 insulin pump with Basal-IQ technology; t: slim…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tandem Diabetes Care Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 5, 2022
Dutch Red Potatoes with Dijon Mustard Sauce. NET WT. 1 LB 1.7 OZ (502g) UPC code 0-45255-15221-0 Distributed by World…
High riskUsing this product could cause serious injury, illness or death — stop using it now.World Variety Produce Inc. dba Melissa's
FDA (openFDA food enforcement)
Reported Sep 28, 2022
BD MaxGuard Extension Set with 4-way stopcock, REF: M4058
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carefusion
8 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 28, 2022
AquaC UNO H [120V, 60Hz, 1000VA, US-Version - a reverse osmosis unit intended for use with hemodialysis systems.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Medical Care Holdings, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 28, 2022
Grappler Suture Anchor, Titanium, 3.0 x 10mm, Sterile Kit, REF: P44-110-3010-SK, for use within the Grappler Suture…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Paragon 28, Inc.
FDA (openFDA device enforcement)
Reported Sep 21, 2022
MicroClave Clear Neutral Connector. A bidirectional connector used as an accessory to an intravascular catheter placed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 21, 2022
Stryker USB Converter, Polaris Spectra Camera, Catalog #201148, a component of the Mako Robotic-Arm Assisted Surgery…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported Sep 21, 2022
QIAcube Connect MDx, Model No. 9003070
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Qiagen Sciences LLC
FDA (openFDA device enforcement)
Reported Sep 21, 2022
Verify SixCess Challenge Pack. Used to confirm that critical parameters of steam sterilization have been reached within…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Steris Corporation Hopkins Facility
FDA (openFDA device enforcement)
Reported Sep 21, 2022
ZAP-X Radiosurgery System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zap Surgical Systems
FDA (openFDA device enforcement)
Reported Sep 14, 2022
Abbott Alinity m SARS-CoV-2 CTRL Kit, REF 09N78-085, each kit contains 12 x 1.3mL CTRL - and 12 x 1.3 mL CTRL +, For In…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Molecular, Inc.
FDA (openFDA device enforcement)
Reported Sep 14, 2022
Various Angiography packs/trays
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Contract Systems, Inc.
16 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 14, 2022
Optima Coil System Model OPTI0520CSF10. For endovascular embolization.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Balt USA, LLC
FDA (openFDA device enforcement)
Reported Sep 14, 2022
CARTO VIZIGO 8.5F Bi-Directional Guiding Sheath, REF: D138501. Used to introduce various cardiovascular catheters into…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biosense Webster, Inc.
FDA (openFDA device enforcement)
Reported Sep 14, 2022
Product Description/Item: ChemoLock Bag Spike, 10 units/CL-10-10; ChemoLock BAG SPIKE w/ ADDITIVE PORT, DRY…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 14, 2022
Orthex External Fixation Wire Sharp Bayonet 1.8 x 400 mm Model: K400-18BN
Moderate riskThis product could cause temporary or reversible health problems — stop using it.OrthoPediatrics Corp.
FDA (openFDA device enforcement)
Reported Sep 14, 2022
Starbucks Vanilla Espresso Triple Shot, 15 oz, 12 bottles per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pepsico Inc.
FDA (openFDA food enforcement)
Reported Sep 14, 2022
Philips BiPAP A30, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Philips Respironics, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 14, 2022
Early Bird Bleed Monitoring System Introducer Sheath Set, REF: FG001-01 (6F), FG001-02 (8F)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Saranas, Inc.
FDA (openFDA device enforcement)
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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.