State

Colorado product recalls

20,371 recalls have nationwide distribution and so reach Colorado. 0 additional recalls listed Colorado specifically in their distribution scope.

About recalls in Colorado

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Colorado consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

15351–15375 of 20371

HighFDA (Devices)·Z-0084-2023·2022-10-19
Prismaflex ST Renal Therapy Sets Recalled for Mistranslated Safety Instructions
Baxter Healthcare is recalling 1,068,560 Prismaflex ST renal replacement therapy sets nationwide. The recall is due to a mistranslation in the Estonian instructions that contains contradictory information about patient weight restrictions.
Product
Prismaflex ST Set: ST60 (product code 107643), ST100 (product code 107636), ST150 (product code 107640). For use in providing continuous fluid management and renal replacement therapies.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0041-2023·2022-10-19
Hobbs Medical Recalls Biliary Stent Kits Due to Mislabeled Expiration Dates
Hobbs Medical, Inc. is recalling Biliary Pigtail Stent Kits with incorrect expiration dates displayed on device labels. Affected devices distributed from March 2018 through September 2020 may be used beyond their validated shelf life.
Product
Hobbs Biliary Pigtail Stent Kits (contains 3412) Catalog Number: 6027
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0062-2023·2022-10-19
Freeman Pancreatic Flexi-Stent recalled for incorrect expiration date labeling
Hobbs Medical is recalling Freeman Pancreatic Flexi-Stent devices due to incorrect expiration dates on product labels. The labeling error extends the stated shelf life, potentially allowing use of degraded devices.
Product
Freeman Pancreatic Flexi-Stent Catalog Number: 6567
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0052-2023·2022-10-19
Freeman Pancreatic Flexi-Stent Kit Recalled for Mislabeled Expiration Dates
Hobbs Medical recalls Freeman Pancreatic Flexi-Stent kits with incorrect expiration dates on the label, which extends the stated shelf life and could allow use of expired devices.
Product
Freeman Pancreatic Flexi-Stent Kit (containing 6566) Catalog Number: 6518
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0031-2023·2022-10-19
Hobbs Helical Retrieval Basket recalled for incorrect expiration date
Hobbs Medical recalled 10 units of its Helical Retrieval Basket due to mislabeled expiration dates that extend the product's shelf life, affecting devices distributed in the US and select countries between 2018 and 2020.
Product
Hobbs Helical Retrieval Basket Catalog Number: 4824
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0035-2023·2022-10-19
Hobbs Medical Grasping Forceps Recalled for Incorrect Expiration Dates
Hobbs Medical Grasping Forceps (Catalog 5008) were distributed with incorrect expiration dates that extend shelf life beyond the device's actual safe use period. Affected units with lot numbers ending in 'R' were distributed from March 2018 to September 2020.
Product
Hobbs Medical Grasping Forceps Catalog Number: 5008
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0042-2023·2022-10-19
Hobbs Biliary Pigtail Stent Kit Label Bears Incorrect Expiration Date
Hobbs Medical is recalling Biliary Pigtail Stent Kits due to incorrect expiration dates on device labels that extend shelf life beyond actual product expiration, potentially resulting in use of expired devices.
Product
Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number: 6028
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0049-2023·2022-10-19
Freeman Pancreatic Flexi-Stent Kits recalled for incorrect expiration dates
Hobbs Medical recalls Freeman Pancreatic Flexi-Stent Kits due to mislabeled expiration dates that may extend shelf life. Affected devices with lot numbers ending in R were distributed in the US and internationally from 2018-2020.
Product
Freeman Pancreatic Flexi-Stent Kits: Single Pigtail Catalog Number: 6501
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0051-2023·2022-10-19
Freeman Pancreatic Flexi-Stent Kit Recalled for Mislabeled Expiration Date
Hobbs Medical recalls Freeman Pancreatic Flexi-Stent Kit units with incorrect expiration dates on labels, extending apparent shelf life. Units distributed in the US and Canada, Austria, Belgium, Finland, and Norway from 2018–2020 are affected.
Product
Freeman Pancreatic Flexi-Stent Kit (containing 6533) Catalog Number: 6507
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0082-2023·2022-10-19
Prismaflex M Set Medical Device Recalled Due to Instruction Mistranslation
Baxter Healthcare is recalling 334,932 Prismaflex M Set M150 devices due to a mistranslation in instructions that creates contradictory information about patient body weight restrictions.
Product
Prismaflex M Set: M150 (product code 109990). For use in providing continuous fluid management and renal replacement therapies.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0054-2023·2022-10-19
Freeman Pancreatic Flexi-Stent Kit: Incorrect Expiration Date on Device Labels
Hobbs Medical recalls Freeman Pancreatic Flexi-Stent Kits with incorrect expiration dates on labels that may extend shelf life beyond the actual expiration date.
Product
Freeman Pancreatic Flexi-Stent Kit (containing 6568) Catalog Number: 6529
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0056-2023·2022-10-19
Freeman Pancreatic Flexi-Stent Medical Device Recalled for Mislabeled Expiration Date
Hobbs Medical recalls Freeman Pancreatic Flexi-Stent devices with incorrect expiration dates that extend shelf life, affecting devices distributed in the US and five other countries from 2018 to 2020.
Product
Freeman Pancreatic Flexi-Stent Catalog Number: 6534
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0012-2023·2022-10-19
Hobbs Medical Flex-Ez Guide Wire With Incorrect Expiration Date
Hobbs Medical Flex-Ez Guide Wire devices were labeled with an incorrect expiration date that extends shelf life beyond the intended duration. Affected devices were distributed in the US and internationally from March 2018 to September 2020.
Product
Hobbs Medical Flex-Ez Guide Wire Disposable For endoscopy procedures Ref: 3412
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0061-2023·2022-10-19
Freeman Pancreatic Flexi-Stent Recall Due to Incorrect Expiration Dates
Hobbs Medical recalled Freeman Pancreatic Flexi-Stent devices due to incorrect expiration dates on labels that extend the shelf life, potentially allowing use beyond intended timeframe.
Product
Freeman Pancreatic Flexi-Stent Catalog Number: 6566
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0069-2023·2022-10-19
Hobbs Medical Polypectomy Snare with Incorrect Expiration Date Label
Hobbs Medical is recalling Polypectomy Snare model 4565-OLY due to incorrect expiration dates on device labels that extend the product's shelf life. Affected devices were distributed between March 2018 and September 2020.
Product
Hobbs Medical Polypectomy Snare Catalog Number: 4565-OLY
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0037-2023·2022-10-19
Hobbs Biliary Pigtail Stent Kits recalled due to incorrect expiration dates
Hobbs Medical is recalling certain Biliary Pigtail Stent Kits due to incorrect expiration dates on device labels that extend shelf life beyond actual validity. Affected devices distributed between March 2018 and September 2020 may be used beyond their true expiration date.
Product
Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number: 6001
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0078-2023·2022-10-19
Olympus VC-10 Vacuum Curettage System Recalled for Incompatible Accessories
Olympus recalls the VC-10 Vacuum Curettage System due to serious injury risk from incompatible collection canisters. The FDA warns users against using accessories not listed in the device's instructions.
Product
Berkeley VC-10 Vacuum Curettage System, Model No. VC-10. For transcervical aspiration of the uterine cavity.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0055-2023·2022-10-19
Freeman Pancreatic Flexi-Stent Recalled for Incorrect Expiration Date
Hobbs Medical recalled Freeman Pancreatic Flexi-Stents due to incorrect expiration dates on device labels. The mislabeled dates extend shelf life, potentially allowing use of expired devices.
Product
Freeman Pancreatic Flexi-Stent Catalog Number: 6533
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0022-2023·2022-10-19
Hobbs Posi-Stop Injection Needle Recall - Incorrect Expiration Date
Hobbs Medical is recalling Posi-Stop Injection Needles due to incorrect expiration dates on device labels that extend shelf life. Devices distributed between March 2018 and September 2020 could be used beyond their actual expiration.
Product
Hobbs Posi-Stop Injection Needle Catalog Number: 4712
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-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-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-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