State

Alaska product recalls

73,092 recalls have nationwide distribution and so reach Alaska. 1,765 additional recalls listed Alaska specifically in their distribution scope.

What the numbers show

Total: 1,765
Critical: 118
Severe: 350
Most recent: 2026-09-23

Of the 1,765 recalls naming Alaska we have scored against our rubric, 118 (7%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 350 (20%) are Severe.

Which agencies issued them

These figures cover only the 1,765 recalls whose distribution notice names Alaska specifically. The 73,092 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9001–9025 of 74857

HighFDA (Devices)·Z-0345-2025·2024-11-20
Imed EVA IV bags recalled for leaking during filling
The Metrix Company is recalling Imed EVA IV bags due to leakage discovered during the filling process. A limited number of bags were found to leak, potentially affecting the safety of intravenous therapy.
Product
Imed Products Imed EVA BAG, 1000 mL, 2-PORTS, REF IM68055; 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-0417-2025·2024-11-20
Halyard MINOR PACK Medical Kits Recalled for Loose Metal Fragments in Instruments
AVID Medical is recalling Halyard MINOR PACK medical kits because sponge forceps and towel clamps may shed loose metal fragments. These could enter surgical sites undetected, potentially causing local or foreign body reactions.
Product
Halyard MINOR PACK - Medical convenience kits Model Number: MMOK013-03
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0346-2025·2024-11-20
Cook Approach CTO Micro Wire Guide recalled for incorrect expiration date labels
Cook Incorporated is recalling Approach CTO Micro Wire Guide devices due to incorrect expiration dates on affected lot labels. The recall affects 2,005 units in the US and 1,145 units overseas.
Product
Approach CTO Micro Wire Guide, Guide Wire, Catalog Prefix CMW; Reference Part Numbers: CMW-14-190-12G CMW-14-190-18G CMW-14-190-25G CMW-14-190-6G CMW-14-300-12G CMW-14-300-18G CMW-14-300-25G CMW-14-300-6G
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0461-2025·2024-11-20
MEERA CL operating table may stop unexpectedly during surgical procedures
The MEERA CL operating table may experience error code 50037 on its IR-Hand Control, causing the table to stop mid-procedure. No injuries have been reported.
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: 710001B2
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0352-2025·2024-11-20
Philips Zenition 50 Medical Imaging Device May Experience Electrical Fuse Failure
Philips Zenition 50 imaging systems may experience mains control unit fuse failure during startup or procedures. The defect could cause equipment malfunction.
Product
Philips Zenition 50, Model Number: 718096
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0340-2025·2024-11-20
IV Fluid Container Leak During Filling — SECURE 500 mL EVA Container Recall
The Metrix Company is recalling SECURE 500 mL EVA containers (REF 66050) used for intravenous administration because a limited number have been found to leak during filling. Affected lots were distributed nationwide and to Canada.
Product
SECURE 500 mL EMPTY EVA CONTAINER With 2 Ports, REF 66050; 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-0396-2025·2024-11-20
Halyard SPINE Kit recalled for loose metal flakes in surgical instruments
AVID Medical is recalling Halyard SPINE surgical kits (Model EUOR004-02) due to loose metal flakes that may detach from sponge forceps and towel clamps. These flakes could potentially enter a patient's surgical site, causing local or foreign body reactions.
Product
Halyard KIT, SPINE - Medical convenience kits Model Number: EUOR004-02
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0331-2025·2024-11-20
VYGON 250 mL IV Fluid Containers Recalled for Leaks During Filling
The Metrix Company is recalling VYGON 250 mL IV fluid containers that have been found to leak during filling. Leaking containers cannot properly contain intravenous fluid.
Product
VYGON 250 mL EMPTY EVA CONTAINER With 2 Ports, REF CMS-9602; 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-0338-2025·2024-11-20
IV Fluid Bags Recalled Due to Leakage During Filling
The Metrix Company is recalling SECURE 50 mL empty IV containers due to leakage found during filling. A limited number of affected bags have been distributed nationwide.
Product
SECURE 50 mL EMPTY EVA CONTAINER With 2 Ports (Bulk Packed) , REF 66043; 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-0336-2025·2024-11-20
IV Fluid Bags Found to Leak During Filling; Manufacturer Recalls Affected Units
The Metrix Company is recalling 2549 cases of SECURE 100 mL empty IV fluid bags because a limited number were found to leak during filling, which could result in contamination during fluid administration.
Product
SECURE 100 mL EMPTY EVA CONTAINER With 2 Ports (Bulk Packed), REF 66041; 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-0333-2025·2024-11-20
IV Bag Containers Recalled Due to Leaking During Filling
The FDA has recalled CORMIX 250 mL empty IV bags made by The Metrix Company due to leaking during the filling process. Approximately 3,456 cases were distributed across the US and Canada.
Product
CORMIX 250 mL EMPTY EVA CONTAINER With 2 Ports, REF MS64045; 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-0398-2025·2024-11-20
Halyard FOOT ANKLE PACK surgical instruments recalled due to loose metal flakes
AVID Medical recalls Halyard FOOT ANKLE PACK surgical kits due to loose metal flakes from sponge forceps and towel clamps that could enter surgical sites and cause local reactions.
Product
Halyard FOOT ANKLE PACK - Medical convenience kits Model Number: EUOR005-02
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0434-2025·2024-11-20
Surgical instrument kits recalled for loose metal flakes
AVID Medical is recalling Halyard CPT EP PACK surgical convenience kits due to loose metal flakes on forceps and towel clamps. Detached metal flakes could enter surgical sites and potentially cause local tissue reactions or foreign body complications.
Product
Halyard CPT EP PACK - Medical convenience kits Model Number: SHAN442-04
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0405-2025·2024-11-20
Halyard GYN TRAY surgical kits recalled for loose metal flakes
AVID Medical is recalling 136 units of Halyard GYN TRAY surgical kits due to small loose metal flakes that could detach from sponge forceps and towel clamps. These metal fragments could enter a patient's surgical site undetected, causing local or foreign body reactions.
Product
Halyard GYN TRAY - Medical convenience kits Model Number: LANC014-19
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0397-2025·2024-11-20
Halyard surgical kit recalled for loose metal flakes in forceps and clamps
AVID Medical is recalling Halyard KIT, SPINE surgical convenience kits due to loose metal flakes on sponge forceps and towel clamps. The flakes could detach and enter a patient's surgical site, potentially causing local or foreign body reactions.
Product
Halyard KIT, SPINE - Medical convenience kits Model Number: EUOR004-03
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0465-2025·2024-11-20
Medline Iris Scissors Recalled for Potential Sterility Barrier Compromise
Medline is recalling 69,611 single-use iris scissors because the tip protector may fall off during packaging, compromising the sterile barrier. Affected units were distributed nationwide to 20 states.
Product
Medline Iris Scissors, Single-Use, Curved, Standard 4.5 , Model Nos. DYNJ04049 (cases), DYNJ04049H (eaches)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0450-2025·2024-11-20
Surgical kits recalled for potentially detachable metal flakes
AVID Medical is recalling Halyard VA lumbar laminectomy surgical kits because sponge forceps and towel clamps may have loose metal flakes that could detach and enter a patient's surgical site.
Product
Halyard VA LUMBAR LAMINECTOMY - Medical convenience kits Model Number: VMED009-03
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0386-2025·2024-11-20
ENT surgical kit recalled for potentially detachable metal flakes in forceps
AVID Medical is recalling Halyard ENT T and A Pack surgical kits nationwide due to loose metal flakes in sponge forceps and towel clamps that may contaminate surgical sites.
Product
Halyard ENT T AND A PACK - Medical convenience kits Model Number: EAMC106-02
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0349-2025·2024-11-20
Surgical hip procedure kit recalled for incomplete product seals
Medline is recalling CARROLLTON HIP FX surgical kits due to incomplete seals on items within the kit. Affected units contain Lot Number 24EBP466 and were distributed in Tennessee.
Product
CARROLLTON HIP FX Convenience kit used for surgical procedures, SKU SYNJ910003A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0334-2025·2024-11-20
IV Bag Containers Recalled for Leaking During Filling Process
The Metrix Company is recalling CORMIX 500 mL IV bag containers that may leak during the filling process. These plastic pouches are intended for intravenous fluid administration.
Product
CORMIX 500 mL EMPTY EVA CONTAINER With 2 Ports, REF MS64050; 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-0332-2025·2024-11-20
IV Fluid Containers Recalled for Leakage Risk During Filling
The Metrix Company is recalling CORMIX 150 mL empty IV fluid containers due to leakage found during filling, which could compromise the integrity of intravenous fluids.
Product
CORMIX 150 mL EMPTY EVA CONTAINER With 2 Ports, REF MS64040; 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-0416-2025·2024-11-20
Halyard Extremity Pack Surgical Instruments Recalled for Loose Metal Flakes
AVID Medical recalls Halyard Extremity Pack surgical instruments (model MMOK009-03) because small metal flakes may detach from sponge forceps and towel clamps and enter patients' surgical sites. No injuries have been reported.
Product
Halyard EXTREMITY PACK - Medical convenience kits Model Number: MMOK009-03
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0449-2025·2024-11-20
Halyard ENDOVASCULAR surgical kits recalled for loose metal flakes
Halyard ENDOVASCULAR Model VMED008-02 surgical convenience kits are recalled due to potential loose metal flakes in sponge forceps and towel clamps. These flakes could enter a surgical site and cause local or foreign body reactions.
Product
Halyard ENDOVASCULAR - Medical convenience kits Model Number: VMED008-02
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0400-2025·2024-11-20
Surgical procedure kits recalled due to loose metal flakes in instruments
AVID Medical is recalling Halyard BASIC PROCEDURE PACK surgical instrument kits because sponge forceps and towel clamps may contain loose metal flakes that could enter a patient's surgical site and cause local or foreign body reactions.
Product
Halyard BASIC PROCEDURE PACK - Medical convenience kits Model Number: GRAN019-06
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0419-2025·2024-11-20
Halyard Lower Extremity Pack surgical kits recalled for loose metal fragments
AVID Medical is recalling Halyard Lower Extremity Pack surgical kits because sponge forceps and towel clamps may shed loose metal flakes that could enter a patient's surgical site undetected, potentially causing local or foreign body reactions.
Product
Halyard LOWER EXTREMITY PACK - Medical convenience kits Model Number: PANJ001-03
Category
Medical Device
Distribution
Distributed nationwide