State

Minnesota product recalls

73,100 recalls have nationwide distribution and so reach Minnesota. 7,838 additional recalls listed Minnesota specifically in their distribution scope.

What the numbers show

Total: 7,838
Critical: 1,139
Severe: 1,904
Most recent: 2026-09-23

Of the 7,838 recalls naming Minnesota we have scored against our rubric, 1,139 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,904 (24%) are Severe.

Which agencies issued them

These figures cover only the 7,838 recalls whose distribution notice names Minnesota specifically. The 73,100 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9401–9425 of 80938

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-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-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-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-0330-2025·2024-11-20
VYGON 100 mL IV Container Pouch Recalled for Potential Leakage
The Metrix Company is recalling a limited number of VYGON 100 mL empty IV containers (Lot Numbers 62040-A8375 and 62040-A8432) due to leakage found during the filling process. The affected containers are distributed in multiple U.S. states and Canada.
Product
VYGON 100 mL EMPTY EVA CONTAINER With 2 Ports, REF CMS-9601; 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-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…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0448-2025·2024-11-20
Medical Convenience Kits Recalled for Potential Loose Metal Flakes in Surgical Instruments
AVID Medical is recalling Halyard MANIFOLD CATH PACK medical convenience kits because sponge forceps and towel clamps may shed metal flakes that could contaminate surgical sites.
Product
Halyard MANIFOLD CATH PACK - Medical convenience kits Model Number: VMED005-03
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-0436-2025·2024-11-20
AVID Medical Recalls Halyard GYN PAC Kits Due to Metal Flakes
AVID Medical is recalling Halyard GYN PAC medical convenience kits because sponge forceps and towel clamps may release metal flakes that could enter a patient's surgical site.
Product
Halyard GYN PAC - Medical convenience kits Model Number: SJGY20-02
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0369-2025·2024-11-20
Stryker Neptune SafeAir smoke evacuation pencil recalled for unintended activation
Stryker Corporation is recalling 21,490 Neptune SafeAir Smoke Evacuation Pencils due to risk of unintended activation that could cause electrical burns. The device may activate without user input or remain active after buttons are released.
Product
Stryker Neptune SafeAir Smoke Evacuation Pencil Non coated 70 mm Blade Push-Button - Designed for general electrosurgical applications including cutting and coagulation and for removing smoke generated by electrosurgery when used in conjunction with an effective smoke evacuation…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0367-2025·2024-11-20
Stryker smoke evacuation pencil recall: unintended activation risk
Stryker is recalling Neptune SafeAir Rocker-Switch Smoke Evacuation Pencils due to risk of unintended activation when plugged in or after button release, which may cause localized electrical burns requiring medical intervention.
Product
Stryker Neptune SafeAir Rocker-Switch Smoke Evacuation Pencil, Non-coated, 70mm - Designed for general electrosurgical applications including cutting and coagulation and for removing smoke generated by electrosurgery when used in conjunction with an effective smoke evacuation…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0044-2025·2024-11-20
Lanthanum Carbonate Chewable Tablets Recalled for Crushed and Broken Tablets
Cipla USA is recalling Lanthanum Carbonate Chewable Tablets (1000mg) distributed nationwide due to complaints of crushed and broken tablets that fail manufacturing specifications.
Product
Lanthanum Carbonate Chewable Tablets, 1000mg, 10-count bottle, Rx only, Manufactured for Exelan Pharmaceuticals, NDC 76282-0478-90
Category
Drug
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-0351-2025·2024-11-20
Cystoscope Outer Sheath Recalled for Potential Laser Probe Damage
Olympus is recalling 738 units of the WA22810A Cystoscope Outer Sheath distributed nationwide due to potential damage to the laser probe tip during use with GreenLight Laser for BPH therapy. The manufacturer removed this compatibility claim from product instructions.
Product
Brand Name: Olympus Product Name: Cystoscope Outer Sheath Model/Catalog Number: WA22810A Software Version: N/A Product Description: Outer sheaths can be combined with rigid Telescopes. Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0444-2025·2024-11-20
Halyard IVR Vascular Pack Surgical Instruments Recalled for Loose Metal Components
AVID Medical is recalling Halyard IVR Vascular Pack surgical kits because sponge forceps and towel clamps may shed loose metal flakes that could enter a patient's surgical site.
Product
Halyard IVR VASCULAR PACK - Medical convenience kits Model Number: VAST027-08
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…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0365-2025·2024-11-20
Stryker Neptune SafeAir Electrosurgical Pencil Recalled for Unintended Activation Risk
Stryker has recalled over 1.1 million Neptune SafeAir Smoke Evacuation Pencils due to potential unintended activation that may cause electrical burns to patients and surgical staff. The device may activate without user input or remain active after buttons are released.
Product
Stryker Neptune SafeAir Rocker-Switch Smoke Evacuation Pencil, Coated, 70mm - Designed for general electrosurgical applications including cutting and coagulation and for removing smoke generated by electrosurgery when used in conjunction with an effective smoke evacuation…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0389-2025·2024-11-20
Surgical Instruments Recalled for Loose Metal Flakes in Set-Up Packs
AVID Medical is recalling Halyard GENERAL SET UP PACK medical convenience kits nationwide due to sponge forceps and towel clamps that may shed small metal flakes into patients' surgical sites, risking local reactions and foreign body reactions.
Product
Halyard GENERAL SET UP PACK - Medical convenience kits Model Number: ESJH005-02
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0335-2025·2024-11-20
IV Fluid Container Bags Recalled for Leaking Defect
The Metrix Company is recalling SECURE 100 mL empty EVA containers for IV use due to leaking discovered during filling. Approximately 2,229 cases were distributed to healthcare facilities in the US and Canada.
Product
SECURE 100 mL EMPTY EVA CONTAINER With 2 Ports, REF 66040; 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-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-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-0355-2025·2024-11-20
Medical Laboratory Kit Recalled Due to Non-Sterile Specimen Container
Medline Industries is recalling over 626,000 laboratory kits because the included specimen container is labeled as sterile but is actually non-sterile. Non-sterile containers risk sample contamination and may result in unnecessary treatment or prolonged hospitalization.
Product
Lab Kit, SKU DYLAB1018; Component No. 503581
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0425-2025·2024-11-20
Halyard Urology Laparotomy Pack surgical instruments recalled for detachable metal flakes
AVID Medical recalls Halyard Urology Laparotomy Pack surgical instruments (Model SAMM023-13, Lot 1595070) due to loose metal flakes that could detach from forceps and clamps, potentially entering surgical sites and causing foreign body reactions.
Product
Halyard UROLOGY LAPAROTOMY PACK - Medical convenience kits Model Number: SAMM023-13
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