State

Montana product recalls

73,566 recalls have nationwide distribution and so reach Montana. 3,572 additional recalls listed Montana specifically in their distribution scope.

What the numbers show

Total: 3,572
Critical: 689
Severe: 952
Most recent: 2026-10-14

Of the 3,572 recalls naming Montana we have scored against our rubric, 689 (19%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 952 (27%) are Severe.

Which agencies issued them

These figures cover only the 3,572 recalls whose distribution notice names Montana specifically. The 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26026–26050 of 77138

ModerateFDA (Devices)·Z-1585-2021·2021-05-19
ICU Medical Recalls Spiros Closed Male Luer Due to Leakage Defect
ICU Medical is recalling Spiros Closed Male Luer devices due to a molding defect that may cause leakage in the inactivated position.
Product
REF 20120-01 Spiros" Closed Male Luer - Product Usage: provides access for the administration of fluids from a container to a patient s vascular system through the administration set s needle or catheter (which is inserted into a vein).
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1571-2021·2021-05-19
ICU Medical Recalls Sprios Administration Sets Due to Molding Defect
ICU Medical is recalling specific lots of Sprios administration sets due to a molding defect that may cause leakage in the inactivated position.
Product
REF CL3028T 30" (76 cm) Appx 6.1 ml, 20 Drop Admin Set w/Integrated w/ChemoLock Drip Chamber, 0.2 Micron Filter, Spiros , Bag Hanger, Drop-In Red Cap - Product Usage: provides access for the administration of fluids from a container to a patients vascular system through the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1576-2021·2021-05-19
ICU Medical Recalls 20mL Syringes Due to Potential Leakage Defect
ICU Medical is recalling specific lots of 20mL syringes with Spinning Spiros due to a molding defect that may cause leakage in the inactivated position.
Product
REF CH2020 20mL Syringe w/Spinning Spiros, Red Cap - Product Usage: provides access for the administration of fluids from a container to a patient s vascular system through the administration set s needle or catheter (which is inserted into a vein).
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1569-2021·2021-05-19
ICU Medical Recalls Spinning Spiros Closed Male Luer Due to Leakage
ICU Medical is recalling certain lots of Spinning Spiros Closed Male Luer devices due to a molding defect that may cause leakage in the inactivated position.
Product
REF Spinning Spiros Closed Male Luer - Product Usage: provides access for the administration of fluids from a container to a patients vascular system through the administration sets needle or catheter (which is inserted into a vein).
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1577-2021·2021-05-19
ICU Medical Recalls Spinning Spiros Syringes Due to Leakage Defect
ICU Medical is recalling specific lots of 60mL Spinning Spiros syringes because a molding defect may cause leakage in the inactivated position.
Product
REF CH2060 60mL Syringe w/Spinning Spiros, Red Cap - Product Usage: provides access for the administration of fluids from a container to a patient s vascular system through the administration set s needle or catheter (which is inserted into a vein).
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1567-2021·2021-05-19
ICU Medical Recalls Spiros Administration Sets Due to Molding Defect
ICU Medical is recalling specific lots of Spiros administration sets because a molding defect may cause leakage in the inactivated position.
Product
REF 20124-01 30" (76 cm) Appx 3.2 ml, 20 Drop Admin Set w/Integrated Clave Drip Chamber, Spiros, Bag Hanger LOT 5142971 - Product Usage: provides access for the administration of fluids from a container to a patients vascular system through the administration sets needle or…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0372-2021·2021-05-19
Sun Pharmaceutical Recalls Metformin Hydrochloride Tablets Due to Foreign Substance
Sun Pharmaceutical Industries is recalling 50,868 bottles of Metformin Hydrochloride Extended-Release Tablets because activated carbon was found in the product.
Product
METFORMIN HYDROCHLORIDE — METFORMIN HYDROCHLORIDE (METFORMIN HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1581-2021·2021-05-19
ICU Medical Recalls Admin Sets Due to Potential Leakage Defect
ICU Medical is recalling specific lots of REF 011-CH3967 Admin Sets due to a molding defect that may cause leakage in the inactivated position.
Product
REF 011-CH3967 Admin Set w/ClaveTM, SpirosTM - Product Usage: provides access for the administration of fluids from a container to a patient s vascular system through the administration set s needle or catheter (which is inserted into a vein).
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1588-2021·2021-05-19
ICU Medical Recalls Spiros Administration Sets Due to Molding Defect
ICU Medical is recalling specific lots of Spiros administration sets because a molding defect may cause small amounts of leakage in the inactivated position.
Product
REF CH3235 30" (76 cm) Appx 4.1 ml, Yellow 20 Drop Admin Set w/15 Micron Filter, Spiros" - Product Usage: provides access for the administration of fluids from a container to a patient s vascular system through the administration set s needle or catheter (which is inserted into…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1564-2021·2021-05-19
Medtronic Recalls VenaSeal Closure Systems Due to Adhesive Delivery Issues
Medtronic is recalling 154,152 VenaSeal Closure Systems because the dispensing systems may not effectively advance adhesive through the delivery catheter.
Product
VenaSeal Closure System
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1580-2021·2021-05-19
ICU Medical Recalls Smallbore Trifuse Extension Sets Due to Leakage Defect
ICU Medical is recalling specific lots of Smallbore Trifuse Extension Sets because a molding defect may cause leakage in the inactivated position.
Product
REF CH3625 5" (13 cm) Appx 0.50 ml, Smallbore Trifuse Ext Set w/3 ChemoClave (Purple, Green Rings), Spiros w/Red Cap, 3 Clamps - Product Usage: provides access for the administration of fluids from a container to a patient s vascular system through the administration set s…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1578-2021·2021-05-19
ICU Medical Recalls Sprios Administration Sets Due to Molding Defect
ICU Medical is recalling specific lots of Sprios administration sets due to a molding defect that may cause leakage in the inactivated position.
Product
REF CH3011 30" (76 cm) Appx 3.3 mL, 20 Drop Admin Set w/Integrated ChemoClave Drip Chamber, Spiros w/Red Cap, Bag Hanger - Product Usage: provides access for the administration of fluids from a container to a patient s vascular system through the administration set s needle or…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1572-2021·2021-05-19
ICU Medical Recalls Oncology Kits Due to Molding Defect
ICU Medical is recalling specific lots of REF CL3538 Oncology Kits because a molding defect may cause small amounts of leakage in the inactivated position.
Product
REF CL3538 Oncology Kit w/5" (13 cm) Add-On Set w/ChemoLock Additive Port, Vented Cap; ChemoLock , Spinning Spiros w/Red Cap - Product Usage: provides access for the administration of fluids from a container to a patients vascular system through the administration sets needle…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1565-2021·2021-05-19
ICU Medical Recalls Oncology Kits Due to Molding Defect and Leakage
ICU Medical is recalling specific lots of Oncology Kits due to a molding defect that may cause leakage in the inactivated position.
Product
REF CH3397 Oncology Kit w/Spiros¿, Red Cap, Bag Spike w/Clave Additive Port LOT 5118610 - Product Usage: for use in the preparation and patient administration of cytotoxic medications.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1586-2021·2021-05-19
ICU Medical Recalls Spinning Spiros Male Luers Due to Molding Defect
ICU Medical is recalling specific lots of Spinning Spiros male luers because a molding defect may cause small amounts of leakage in the inactivated position.
Product
REF 20130-01 Spinning Spiros¿ Closed Male Luer, Red Cap REF CH2000S-PC Spinning Spiros¿ Closed Male Luer, Purple Cap - Product Usage: provides access for the administration of fluids from a container to a patient s vascular system through the administration set s needle or…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1590-2021·2021-05-19
ICU Medical Recalls Spinning Spiros Male Luers Due to Leakage Defect
ICU Medical is recalling specific lots of Spinning Spiros Closed Male Luers because a molding defect may cause leakage in the inactivated position.
Product
REF K7040-001 Spinning Spiros Closed Male Luer - Product Usage: provides access for the administration of fluids from a container to a patient s vascular system through the administration set s needle or catheter (which is inserted into a vein).
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1536-2021·2021-05-19
Fresenius AquaBplus Water Purification System Recalled for Installation Error
Fresenius Medical Care is recalling 27 AquaBplus water purification systems because an installation guideline error may reduce the effectiveness of heat disinfection.
Product
AquaBplus and AquaBplus B2 Water Purification System - Product Usage: Intended for use with a hemodialysis system to remove organic and inorganic substances and microbial contaminants from the water used for hemodialysis or related therapies. Fresenius P/N 24-2500-0 All 3…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1560-2021·2021-05-19
Haag-Streit LENSTAR LS900 Software Recall for Data Mixing Errors
Haag-Streit USA Inc is recalling Eyesuite 9.3.1 software for LENSTAR LS900 devices due to potential mixing of patient names and examination data.
Product
Eyesuite 9.3.1 software, LENSTAR, MODEL LS900: ac-powered slit-lamp biomicroscope.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1587-2021·2021-05-19
ICU Medical Recalls Bag Spike Adapters Due to Molding Defect
ICU Medical is recalling specific lots of Bag Spike Adapters due to a molding defect that may cause leakage in the inactivated position.
Product
REF CH3034 5" (13 cm) Bag Spike Adapter w/Spiros" w/Red Cap, Vented Cap - Product Usage: provides access for the administration of fluids from a container to a patient s vascular system through the administration set s needle or catheter (which is inserted into a vein).
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1575-2021·2021-05-19
ICU Medical Recalls Smallbore Extension Sets Due to Molding Defect
ICU Medical is recalling specific lots of smallbore extension sets because a molding defect may cause leakage in the inactivated position.
Product
REF CL4151 45" (114 cm) Appx 1.7 ml, Smallbore Ext Set w/Spiros w/Red Cap, Anti-Siphon Valve, Clamp, Y-Connector w/ChemoLock Port, Rotating Luer - Product Usage: provides access for the administration of fluids from a container to a patient s vascular system through the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1561-2021·2021-05-19
Remel Bile Esculin Azide Agar Recalled for Growth of E. faecalis
Remel Inc is recalling Bile Esculin Azide Agar with Vancomycin because the media allows growth of E. faecalis ATCC 29212.
Product
Remel Bile Esculin Azide Agar w/ 6mcg/ml Vancomycin, Product #R01186, 10/package - Product Usage: use in qualitative procedures as a screening method for primary isolation and presumptive identification of vancomycin-resistance enterococci (VRE) from surveillance cultures.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1589-2021·2021-05-19
ICU Medical Recalls IV Administration Sets Due to Molding Defect
ICU Medical is recalling specific lots of IV administration sets because a molding defect may cause leakage in the inactivated position.
Product
REF CH3762 35" (89 cm) Appx 3.9 ml, 10 Drop Admin Set w/Integrated Clave" Drip Chamber, Clave", Spiros" w/Red Cap, Bag Hanger - Product Usage: provides access for the administration of fluids from a container to a patient s vascular system through the administration set s…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1562-2021·2021-05-19
Musculoskeletal Transplant Foundation Recalls AFT Straight Tubes Due to Filling Error
Musculoskeletal Transplant Foundation is recalling AFT Straight Tubes that were filled only halfway instead of three-quarters, which may cause surgery delays.
Product
AFT Straight Tube (3/4 Filled) - Human Allograph Tissue for treatment of surgically-created osseous defects or osseous defects created from traumatic injury. It can be used in the: extremities, pelvis, and spine Item Number: 227007
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1574-2021·2021-05-19
ICU Medical Recalls Oncology Kits Due to Potential Leakage Defect
ICU Medical is recalling specific lots of Oncology Kits because a molding defect may cause small amounts of leakage in the inactivated position.
Product
REF CL3960 Oncology Kit w/60" (152 cm) Appx 2.2 ml, Smallbore Ext Set w/w/ChemoLock Port, Clamp, Anti-Siphon Valve, Spiros ; w/ChemoLock; Syringe Transfer Set w/MicroClave, w/ChemoLock Port - Product Usage: provides access for the administration of fluids from a container to a…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V364000·2021-05-18
MCI Recalls Diesel Buses Due to Fuel Rail Leak Fire Risk
Motor Coach Industries is recalling specific 2017-2021 MCI diesel buses because a fuel rail leak could cause a fire.
Product
MCI — MCI D4000, J4500, D4505, D4500
Category
Vehicle
Distribution
Distributed nationwide