State

Montana product recalls

73,366 recalls have nationwide distribution and so reach Montana. 3,571 additional recalls listed Montana specifically in their distribution scope.

What the numbers show

Total: 3,571
Critical: 689
Severe: 952
Most recent: 2026-09-23

Of the 3,571 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 3,571 recalls whose distribution notice names Montana specifically. The 73,366 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19326–19350 of 76937

HighFDA (Devices)·Z-0050-2023·2022-10-19
Freeman Pancreatic Flexi-Stent Kits Recalled Due to Incorrect Expiration Dates
Freeman Pancreatic Flexi-Stent Kits are recalled due to device labels displaying incorrect expiration dates that extend shelf life. Affected units were distributed in the US and select countries from March 2018 to September 2020.
Product
Freeman Pancreatic Flexi-Stent Kits: Single Pigtail (containing 6544) Catalog Number: 6503
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0060-2023·2022-10-19
Freeman Pancreatic Flexi-Stent Recall Due to Incorrect Expiration Date
Hobbs Medical is recalling Freeman Pancreatic Flexi-Stent devices due to incorrect expiration dates on product labels. The incorrect dates extend the shelf life, potentially allowing use beyond the actual safe expiration.
Product
Freeman Pancreatic Flexi-Stent Catalog Number: 6562
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0032-2023·2022-10-19
Hobbs Helical Retrieval Basket Recall Due to Incorrect Expiration Date Label
Hobbs Medical is recalling Hobbs Helical Retrieval Basket (Catalog Number 4830) due to an incorrect expiration date on the device label. Affected devices have lot numbers ending in 'R' and were distributed in the US from March 2018 to September 2020.
Product
Hobbs Helical Retrieval Basket Catalog Number: 4830
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0046-2023·2022-10-19
Freeman Pancreatic Flexi-Stent Kit recalled for incorrect expiration date labeling
Hobbs Medical recalls the Freeman Pancreatic Flexi-Stent Kit due to incorrect expiration dates on product labels that extend shelf life. Affected devices were distributed to the US and international markets from March 2018 through September 2020.
Product
Freeman Pancreatic Flexi-Stent Kit (containing 6352) Catalog Number: 6321
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0023-2023·2022-10-19
Hobbs Posi-Stop Injection Needle recalled for incorrect expiration date on label
Hobbs Medical is recalling Posi-Stop Injection Needles (lot numbers ending in R) due to incorrect expiration dates on labels that extend shelf life. Affected devices were distributed in the US from March 2018 to September 2020.
Product
Hobbs Posi-Stop Injection Needle Catalog Number: 4718
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0027-2023·2022-10-19
Hobbs Helical Retrieval Basket Recalled for Incorrect Expiration Date Labels
Hobbs Medical is recalling Helical Retrieval Baskets with incorrect expiration dates that extend shelf life. Devices distributed from March 2018 through September 2020 may be used beyond their safe operating period.
Product
Hobbs Helical Retrieval Basket Catalog Number: 4808
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0020-2023·2022-10-19
Hobbs Posi-Stop Injection Needle Recalled for Incorrect Expiration Date Labeling
Hobbs Medical is recalling Hobbs Posi-Stop Injection Needles with certain lot numbers because device labels display an incorrect expiration date, extending the product's indicated shelf life.
Product
Hobbs Posi-Stop Injection Needle Catalog Number: 4702
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0028-2023·2022-10-19
Medical Device Retrieval Basket Recalled for Incorrect Expiration Date
Hobbs Medical is recalling Helical Retrieval Baskets with incorrect expiration dates on labels. The labeled shelf life extends beyond the actual safe duration for device use.
Product
Hobbs Helical Retrieval Basket Catalog Number: 4814
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0021-2023·2022-10-19
Hobbs Posi-Stop Injection Needle recalled for incorrect expiration dates
Hobbs Medical is recalling Hobbs Posi-Stop Injection Needles due to incorrect expiration dates on device labels that extend the shelf life. Affected devices have lot numbers ending in 'R' distributed from 2018–2020.
Product
Hobbs Posi-Stop Injection Needle Catalog Number: 4704
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0038-2023·2022-10-19
Hobbs Biliary Pigtail Stent Kits recalled due to incorrect expiration date
Hobbs Medical is recalling Biliary Pigtail Stent Kits with incorrect expiration dates on labels. The incorrect dates extend the product shelf life, potentially allowing devices to be used past their actual expiration.
Product
Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number:6004
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0068-2023·2022-10-19
Hobbs Medical Polypectomy Snare Recalled for Incorrect Expiration Dates
Hobbs Medical is recalling polypectomy snares with incorrect expiration dates on labels. Affected devices have lot numbers ending in R and were distributed from March 2018 to September 2020.
Product
Hobbs Medical Polypectomy Snare Catalog Number: 4563-OLY
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0029-2023·2022-10-19
Hobbs Helical Retrieval Basket Recall: Incorrect Device Label Expiration Date
Hobbs Medical is recalling Helical Retrieval Baskets due to incorrect expiration dates on device labels. The mislabeling extends the shelf life, potentially allowing use of expired devices.
Product
Hobbs Helical Retrieval Basket Catalog Number: 4816
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0083-2023·2022-10-19
Prismaflex HF medical device sets recalled for instructional mistranslation
Baxter Healthcare recalls Prismaflex HF Set devices due to a mistranslation in Estonian language instructions. The mistranslation contains contradictory information about patient body weight restrictions.
Product
Prismaflex HF Set: HF1000 (product code 107140), HF1400 (product code 107142). For use in providing continuous fluid management and renal replacement therapies.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0014-2023·2022-10-19
Hobbs Medical Cytology Brush Recalled for Incorrect Expiration Date Labeling
Hobbs Medical is recalling Cytology Brush Catalog Number 4206 due to incorrect expiration dates on product labels that extend the intended shelf life. Approximately 300 units were distributed nationwide and internationally between March 2018 and September 2020.
Product
Hobbs Medical Cytology Brush Catalog Number: 4206
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0048-2023·2022-10-19
Freeman Pancreatic Flexi-Stent Kit recalled for mislabeled expiration dates
Hobbs Medical is recalling the Freeman Pancreatic Flexi-Stent Kit because the device label displays an incorrect expiration date that extends the shelf life. U.S. distribution of affected devices occurred between March 25, 2018 and September 28, 2020.
Product
Freeman Pancreatic Flexi-Stent Kit Catalog Number: 6352
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0033-2023·2022-10-19
Hobbs Helical Retrieval Basket Recalled for Incorrect Expiration Date
Hobbs Medical, Inc. is recalling Hobbs Helical Retrieval Baskets with lot numbers ending in R due to incorrect expiration dates on device labels. Affected units were distributed worldwide from March 2018 to September 2020.
Product
Hobbs Helical Retrieval Basket Catalog Number: 4832
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0080-2023·2022-10-19
Clip COVID Rapid Antigen Test Kit Recalled for Unapproved Shelf-Life Extension
LUMINOSTICS recalled Clip COVID test kits because the manufacturer extended shelf life and expiration dates without FDA approval. The extended expiration dates lack FDA validation.
Product
Clip COVID Rapid Antigen Test Kit (25-pack), Catalog Number: MDL002
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0057-2023·2022-10-19
Freeman Pancreatic Flexi-Stent Recall Due to Incorrect Expiration Date Label
Hobbs Medical is recalling Freeman Pancreatic Flexi-Stent devices with incorrect expiration dates on labels. Affected units distributed in the US and internationally from 2018 to 2020 may have extended shelf lives beyond accuracy.
Product
Freeman Pancreatic Flexi-Stent Catalog Number: 6535
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0011-2023·2022-10-19
Hobbs Medical Spray Catheter Recalled for Incorrect Expiration Date on Label
Hobbs Medical Spray Catheter devices sold between March 2018 and September 2020 have incorrect expiration dates on their labels. The error may extend the device's shelf life beyond its actual expiration.
Product
Hobbs Medical Spray Catheter: The Mistifier: 2.6mm 165cm Disposable For endoscopy procedures Ref: 2191
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0063-2023·2022-10-19
Pancreatic stent recall due to incorrect expiration date on device labels
Hobbs Medical is recalling Freeman Pancreatic Flexi-Stent devices distributed between March 2018 and September 2020 due to incorrect expiration dates on product labels. The mislabeled devices display extended shelf-life information that does not reflect actual product safety.
Product
Freeman Pancreatic Flexi-Stent Catalog Number: 6568
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0085-2023·2022-10-19
Prismaflex HF20 Medical Device Recall Due to Mistranslated Instructions
Baxter Healthcare recalls the Prismaflex HF20 Set due to a mistranslation in device instructions that creates contradictory information about patient weight restrictions. The issue affects 29,764 devices distributed nationwide.
Product
Prismaflex HF20 Set (product code 109841). For use in providing continuous fluid management and renal replacement therapies.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·22V782000·2022-10-18
PACCAR Recalls 2023 Kenworth and Peterbilt Trucks for Steering Defect
PACCAR is recalling 2023 Kenworth and Peterbilt trucks because improperly heat-treated tie rod clamps may fail, causing a sudden loss of steering.
Product
KENWORTH — KENWORTH, PETERBILT T800B, W900, T370, T480
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22E089000·2022-10-18
Comoto Recalls Youth Helmets for Inadequate Impact Protection
Comoto is recalling specific Bilt Grommet Youth helmets that may not adequately protect the wearer during a crash.
Product
EQUIPMENT:MOTORCYCLE:HELMETS recall
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·22V781000·2022-10-18
Harley-Davidson Touring and Trike Motorcycles Unintended Brake Light Illumination Recall
Harley-Davidson is recalling certain 2019-2022 Touring, Trike, and CVO models due to a software error causing brake lights to illuminate without rider input. This malfunction may confuse other drivers and increase crash risk.
Product
HARLEY-DAVIDSON — HARLEY-DAVIDSON FLTRXS, FLTRXSE, FLTRXST, FLHTCUTGSE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V778000·2022-10-17
Spartan Fire Recalls Emergency Vehicles Due to Tie Rod Clamp Defect
Spartan Fire is recalling 2021-2023 emergency vehicles because improperly heat-treated tie rod clamps may fail, causing loss of steering.
Product
SPARTAN FIRE — SPARTAN FIRE, KME METROSTAR, GLADIATOR, FC-94, redundant PANTHER
Category
Vehicle
Distribution
Distributed nationwide