State

North Dakota product recalls

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

About recalls in North Dakota

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 North Dakota 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.

15326–15350 of 20364

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-0081-2023·2022-10-19
Prismaflex M Set Recall for Mistranslated Weight Restriction Instructions
Baxter Healthcare is recalling Prismaflex M Sets (524,376 devices nationwide) due to a mistranslation in instructions for use that provides contradictory patient body weight restrictions for renal replacement therapy.
Product
Prismaflex M Set: M60 (product code 106696), M100 (product code 106697). 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-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-0053-2023·2022-10-19
Freeman Pancreatic Flexi-Stent Kits Recalled for Incorrect Expiration Dates
Hobbs Medical recalls Freeman Pancreatic Flexi-Stent Kits due to labeling errors showing incorrect expiration dates that extend the shelf life of affected devices.
Product
Freeman Pancreatic Flexi-Stent Kit (containing 6567) Catalog Number: 6519
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-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-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-0044-2023·2022-10-19
Biliary Pigtail Stent Kits Recalled Due to Incorrect Expiration Date Labels
Hobbs Medical recalls Biliary Pigtail Stent Kits with labeling showing incorrect expiration dates that extend the shelf life. Affected kits were distributed to US and international customers from March 2018 to September 2020.
Product
Hobbs Biliary Pigtail Stent Kits Catalog Number: 6105
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-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
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-0070-2023·2022-10-19
Hobbs Medical Polypectomy Snare Incorrect Expiration Date Label Recall
Hobbs Medical polypectomy snares have incorrect expiration dates on labels that extend the device shelf life beyond safe limits. Affected products distributed from March 2018 to September 2020 may be used past their intended expiration.
Product
Hobbs Medical Polypectomy Snare Catalog Number: 4575-OLY
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-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-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-0026-2023·2022-10-19
Medical device retrieval basket labels show incorrect expiration dates
Hobbs Medical recalls the Helical Retrieval Basket due to labels displaying incorrect expiration dates that extend the device's shelf life. Affected units distributed worldwide from March 2018 to September 2020 may be used beyond their validated lifespan.
Product
Hobbs Helical Retrieval Basket Catalog Number: 4806
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0067-2023·2022-10-19
Hobbs Medical Polypectomy Snare with Incorrect Expiration Date Label
Hobbs Medical is recalling Polypectomy Snares (Catalog 7202) with incorrect expiration dates on labels, which could allow use of expired devices. Units were distributed in the US and several other countries from March 2018 to September 2020.
Product
Hobbs Medical Polypectomy Snare Catalog Number: 7202
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-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-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-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-0025-2023·2022-10-19
Hobbs Posi-Stop Injection Needle recalled for incorrect expiration date labeling
Hobbs Medical recalled Posi-Stop Injection Needles with incorrect expiration dates on labels, potentially allowing use of units past actual expiration. The recall affects 17 units distributed in the US and several countries.
Product
Hobbs Posi-Stop Injection Needle Catalog Number: 4722
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