State

Oklahoma product recalls

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

About recalls in Oklahoma

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 Oklahoma 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-0017-2023·2022-10-19
Hobbs Transbronchial Aspiration Needle Recalled for Incorrect Expiration Date
Hobbs Medical is recalling transbronchial aspiration needles with incorrect expiration dates on labels. The 18 affected units were distributed in the US, Canada, Austria, Belgium, Finland, and Norway from March 2018 to September 2020.
Product
Hobbs Transbronchial Aspiration Needle and Vacu-lok Aspirating Syringe Catalog Number: 4620
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-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-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-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-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-0015-2023·2022-10-19
Hobbs Medical Polypectomy Snare recalled for incorrect expiration date on label
Hobbs Medical is recalling its Polypectomy Snare for an incorrect expiration date on the label that extends shelf life. Affected devices were distributed in the US and other countries from March 2018 to September 2020.
Product
Hobbs Medical Polypectomy Snare Catalog Number: 4563
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-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-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-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-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-0030-2023·2022-10-19
Hobbs Helical Retrieval Basket Recall Due to Incorrect Expiration Date
Hobbs Medical is recalling Helical Retrieval Baskets (Catalog 4822) with incorrect expiration dates on device labels. The mislabeled dates extend the shelf life, risking use of expired devices that may not perform as intended.
Product
Hobbs Helical Retrieval Basket Catalog Number: 4822
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-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-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-0066-2023·2022-10-19
Freeman Pancreatic Stent Recall: Incorrect Expiration Date on Device Labels
Freeman Pancreatic Flexi-Stents with incorrect expiration dates on labels may be used beyond their validated shelf life. The recall affects devices distributed in the US and five other countries from March 2018 through September 2020.
Product
Freeman Pancreatic Flexi-Stent (contained in kit 6501) Catalog Number: 6541
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0034-2023·2022-10-19
Hobbs Medical Grasping Forceps Recalled for Incorrect Expiration Date Labeling
Hobbs Medical, Inc. is recalling Grasping Forceps due to incorrect expiration dates on device labels. Affected devices may be used beyond their safe shelf life if the mislabeled expiration dates are not corrected.
Product
Hobbs Medical Grasping Forceps Catalog Number:5004
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0039-2023·2022-10-19
Hobbs Biliary Pigtail Stent Kits recalled for incorrect expiration date
Hobbs Medical recalls biliary stent kits with incorrect expiration dates that extend shelf life. The kits were distributed from 2018 to 2020 in the US and select countries.
Product
Hobbs Biliary Pigtail Stent Kits (containing 6105) Catalog Number: 6023
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-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-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-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-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-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