State

Maine product recalls

20,364 recalls have nationwide distribution and so reach Maine. 0 additional recalls listed Maine specifically in their distribution scope.

About recalls in Maine

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 Maine 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 20364

HighFDA (Devices)·Z-0010-2023·2022-10-19
Hobbs Medical Spray Catheter Recalled for Incorrect Expiration Date
Hobbs Medical is recalling Spray Catheter devices due to incorrectly labeled expiration dates that extend shelf life beyond the actual safe-use period. The recall affects 275 units distributed between March 2018 and September 2020.
Product
Hobbs Medical Spray Catheter: The Mistifier: 2.6mm 260cm Disposable For endoscopy procedures Ref: 2190
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0036-2023·2022-10-19
Hobbs Retrieval Forceps Recalled for Incorrect Expiration Dates
Hobbs Medical is recalling Retrieval Forceps with incorrect expiration dates on device labels. Affected devices distributed between March 2018 and September 2020 may be used past their actual expiration.
Product
Hobbs Retrieval Forceps Catalog Number: 5018
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0018-2023·2022-10-19
Hobbs Medical Transbronchial Aspiration Needle Recalled for Incorrect Expiration Date
Hobbs Medical recalls Transbronchial Aspiration Needle (Catalog 4621) for incorrect expiration dates extending shelf life. Affected devices distributed in the US and internationally from March 2018 to September 2020.
Product
Hobbs Transbronchial Aspiration Needle Catalog Number: 4621
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-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-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-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-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-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-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-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-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-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-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-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-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-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-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
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-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-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-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