State

Arizona product recalls

73,088 recalls have nationwide distribution and so reach Arizona. 8,385 additional recalls listed Arizona specifically in their distribution scope.

What the numbers show

Total: 8,385
Critical: 1,313
Severe: 1,719
Most recent: 2026-09-23

Of the 8,385 recalls naming Arizona we have scored against our rubric, 1,313 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,719 (21%) are Severe.

Which agencies issued them

These figures cover only the 8,385 recalls whose distribution notice names Arizona specifically. The 73,088 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9476–9500 of 81473

HighFDA (Devices)·Z-0372-2025·2024-11-20
Medtronic Recharger Kits Recalled for Potential Failure to Initiate Recharging
Medtronic is recalling 118 wireless recharger kits for implantable neurostimulators because they may fail to start a recharging session upon first use.
Product
Medtronic Recharger Kits, RS6230, RS7230, and RS5220A, containing components WR9230 and WR9220A Recharger for rechargeable implantable neurostimulators. The Rechargers are used with Neurostimulator Inceptiv INS Model 977119 and Percept RC INS Model B35300 as part of the Deep Bra
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0403-2025·2024-11-20
AVID Medical Recalls Halyard MINOR PDS Medical Convenience Kits
AVID Medical, Inc. is recalling 137 Halyard MINOR PDS medical convenience kits because sponge forceps and towel clamps may release metal flakes into surgical sites.
Product
Halyard MINOR PDS - Medical convenience kits Model Number: GVVA009-06
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0368-2025·2024-11-20
Stryker Neptune SafeAir Smoke Evacuation Pencil May Activate Unintentionally
Stryker recalls Neptune SafeAir Smoke Evacuation Pencils that may activate without user input, risking electrical burns to patients or healthcare workers. Approximately 1,996,010 units were distributed worldwide.
Product
Stryker Neptune SafeAir Smoke Evacuation Pencil, Coated, 70mm Blade, Push Button Switch - Designed for general electrosurgical applications including cutting and coagulation and for removing smoke generated by electrosurgery when used in conjunction with an effective smoke evacu
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0432-2025·2024-11-20
AVID Medical Recalls Halyard CPT PEDS ADULT CH PACK Surgical Kits
AVID Medical is recalling 81 units of Halyard CPT PEDS ADULT CH PACK surgical kits because sponge forceps and towel clamps may shed metal flakes.
Product
Halyard CPT PEDS ADULT CH PACK - Medical convenience kits Model Number: SHAN431-06
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0439-2025·2024-11-20
AVID Medical Recalls Halyard EP PACK Kits Due to Metal Flakes
AVID Medical, Inc. is recalling Halyard EP PACK medical convenience kits because sponge forceps and towel clamps may release metal flakes that could enter a patient's surgical site.
Product
Halyard EP PACK - Medical convenience kits Model Number: VANW018-06
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0445-2025·2024-11-20
AVID Medical Recalls Halyard Surgical Kits Due to Metal Flakes
AVID Medical is recalling Halyard SPECIALS PACK medical convenience kits because sponge forceps and towel clamps may release metal flakes that could enter a patient's surgical site.
Product
Halyard SPECIALS PACK - Medical convenience kits Model Number: VAST031-08
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0418-2025·2024-11-20
AVID Medical Recalls Heart Cath Lab Kits Due to Metal Flakes
AVID Medical is recalling 411 Heart Cath Lab Kits because sponge forceps and towel clamps may release metal flakes that could enter a patient's surgical site.
Product
Halyard HEART CATH LAB PK, STRL F G - Medical convenience kits Model Number: MSBM003-03
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0341-2025·2024-11-20
Metrix SECURE 1000 mL IV Container Recall Due to Leaking
The Metrix Company is recalling SECURE 1000 mL empty IV containers because a limited number were found to leak during filling.
Product
SECURE 1000 mL EMPTY EVA CONTAINER With 2 Ports, REF 66055; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0429-2025·2024-11-20
AVID Medical Recalls Pacemaker Convenience Kits Due to Metal Flakes
AVID Medical, Inc. is recalling Halyard SAMMC-N pacemaker convenience kits because sponge forceps and towel clamps may shed metal flakes that could enter a patient's surgical site.
Product
Halyard SAMMC-N PACEMAKER - Medical convenience kits Model Number: SAMM065-10
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0411-2025·2024-11-20
AVID Medical Recalls Halyard Line Insertion Packs Due to Metal Flakes
AVID Medical is recalling Halyard Line Insertion Packs because sponge forceps and towel clamps may release metal flakes that could enter a patient's surgical site.
Product
Halyard LINE INSERTION PACK - Medical convenience kits Model Number: MAMC217-18
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0399-2025·2024-11-20
Surgical instrument kits recalled for potential loose metal flake hazard
Halyard abdominal procedure surgical kits may contain loose metal flakes in forceps and clamps that could enter the surgical site. Affected kits have lot number 1590888.
Product
Halyard ABDOMINAL PROCEDURE - Medical convenience kits Model Number: GRAN015-06
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0364-2025·2024-11-20
Olympus UroPass Ureteral Access Sheaths recalled for UV-induced brittleness
Olympus is recalling UroPass Ureteral Access Sheaths because ultraviolet radiation exposure can cause the dilator tip to become brittle and break during surgery or in storage. Approximately 14,093 units have been distributed worldwide.
Product
Brand Name: UroPass Ureteral Access Sheaths Product Name: Ureteral Access Sheaths Model/Catalog Number: 61024BX, 61038BX, 61046BX, 61054BX, 61124BX, 61138BX, 61146BX, 61154BX, 61224BX, 61238BX, 61246BX, 61254BX, 61324BX, 61338BX, 61346BX, 61354BX Software Version: N/A Product
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0388-2025·2024-11-20
Halyard AORTA PACK Surgical Kit Recalled for Loose Metal Flakes
Halyard AORTA PACK surgical kits are recalled because sponge forceps and towel clamps may contain loose metal flakes that could enter a patient's surgical site, causing local or foreign body reactions.
Product
Halyard AORTA PACK - Medical convenience kits Model Number: ESJH004-02
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0452-2025·2024-11-20
Halyard PACK MINOR surgical instrument kits recalled for metal flake contamination
AVID Medical is recalling Halyard PACK MINOR surgical kits due to loose metal flakes that may detach from forceps and towel clamps. These flakes could potentially enter a patient's surgical site, causing local or foreign body reactions.
Product
Halyard PACK, MINOR - Medical convenience kits Model Number: VMED018-02
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0446-2025·2024-11-20
Halyard EP TRAY Surgical Kits Recalled for Loose Metal Flakes
AVID Medical is recalling Halyard EP TRAY surgical convenience kits due to sponge forceps and towel clamps that may shed small metal flakes. These flakes could enter surgical sites, potentially causing local or foreign body reactions.
Product
Halyard EP TRAY - Medical convenience kits Model Number: VAST038-04
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0370-2025·2024-11-20
Stryker Smoke Evacuation Pencils Recalled for Unintended Activation Risk
Stryker is recalling 403,730 Neptune SafeAir Smoke Evacuation Pencil units because they may activate unexpectedly when plugged in, creating a risk of electrical burns to patients and physicians.
Product
Stryker Neptune SafeAir Smoke Evacuation Pencil Coated Push-Button, Bulk Non-sterile - Designed for general electrosurgical applications including cutting and coagulation and for removing smoke generated by electrosurgery when used in conjunction with an effective smoke evacuatio
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0453-2025·2024-11-20
Halyard Pacemaker Tray Surgical Kits Recalled for Loose Metal Flakes
AVID Medical recalls Halyard PACEMAKER TRAY surgical kits nationwide due to potential loose metal flakes that could detach from sponge forceps and towel clamps and contaminate surgical sites.
Product
Halyard PACEMAKER TRAY - Medical convenience kits Model Number: VMPB0003-10
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0391-2025·2024-11-20
Halyard Shoulder Medical Kit recalled for loose metal flakes in surgical components
AVID Medical is recalling Halyard shoulder surgical kits due to loose metal flakes that could detach and enter surgical sites. Metal debris could cause local or foreign body reactions.
Product
Halyard KIT, SHOULDER - Medical convenience kits Model Number: ESJH014-06
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0456-2025·2024-11-20
MEERA CL Mobile Operating Table Control Malfunction Recall
The MEERA CL mobile operating table may experience error code 50037 that stops table movement during use, causing surgical procedure delays. Getinge recalled 342 units distributed worldwide.
Product
MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical interventions, as well as for examination and treatment, Item Number: 720001B0
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0362-2025·2024-11-20
IMAGEnet 6 Ophthalmic Data System Hood Report Display Issue
IMAGEnet 6 ophthalmic software's Hood Report overlay can mislead clinicians about clinical correlations unsupported by evidence. Affects 3,144 units nationwide.
Product
The IMAGEnet 6 Ophthalmic Data System is a software program that is intended for use in the collection, storage and management of digital images, patient data, diagnostic data and clinical information from Topcon devices. It is intended for processing and displaying ophthalmic
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0447-2025·2024-11-20
Halyard Angiography Drape Pack Recalled for Potential Metal Flakes in Surgical Site
AVID Medical recalls Halyard angiography drape packs due to potential metal flakes that could detach from sponge forceps and towel clamps. These flakes could enter a surgical site undetected and cause local or foreign body reactions.
Product
Halyard ANGIOGRAPHY DRAPE PACK - Medical convenience kits Model Number: VMCC021-06
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0440-2025·2024-11-20
Halyard Biopsy Pack surgical instruments recalled due to loose metal flakes
AVID Medical is recalling Halyard BIOPSY PACK surgical kits due to loose metal flakes from sponge forceps and towel clamps. Metal flakes could enter a patient's surgical site, potentially causing local or foreign body reactions.
Product
Halyard BIOPSY PACK - Medical convenience kits Model Number: VANW019-04
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0442-2025·2024-11-20
Halyard Pacemaker Instrument Packs Recalled for Loose Metal Flakes
AVID Medical is recalling Halyard Pacemaker Instrument Packs (Model VAPX040-01) because sponge forceps and towel clamps may contain loose metal flakes that could detach and enter a patient's surgical site during procedures.
Product
Halyard PACEMAKER INSTRUMENT PACK - Medical convenience kits Model Number: VAPX040-01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0441-2025·2024-11-20
Halyard Angio Tray surgical kits recalled for loose metal flakes
AVID Medical recalls Halyard ANGIO TRAY (Model VAPX021-05) surgical kits due to potential loose metal flakes on forceps and clamps that could enter surgical sites and cause local or foreign body reactions.
Product
Halyard ANGIO TRAY - Medical convenience kits Model Number: VAPX021-05
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0438-2025·2024-11-20
Surgical instruments recalled for loose metal flake contamination risk
AVID Medical is recalling Halyard RAD PACK medical convenience kits containing sponge forceps and towel clamps. Small metal flakes may detach and enter surgical sites, potentially causing foreign body or local tissue reactions.
Product
Halyard RAD PACK - Medical convenience kits Model Number: VANW017-04
Category
Medical Device
Distribution
Distributed nationwide