State

Arkansas product recalls

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

About recalls in Arkansas

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 Arkansas 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-0016-2023·2022-10-19
Hobbs Medical Polypectomy Snare Recalled for Incorrect Expiration Date
Hobbs Medical is recalling Polypectomy Snare devices (Catalog Number 4564) due to incorrect expiration dates on labels that extend the stated shelf life. The 35 affected units, distributed in the US and select countries, may be used beyond their actual safe shelf life.
Product
Hobbs Medical Polypectomy Snare Catalog Number: 4564
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-0040-2023·2022-10-19
Hobbs Biliary Pigtail Stent Kits Recalled for Incorrect Expiration Date Labels
Hobbs Medical is recalling Biliary Pigtail Stent Kits for incorrect expiration dates on product labels that may extend shelf life. Affected kits were distributed nationwide and internationally between March 2018 and September 2020.
Product
Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number: 6024
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0059-2023·2022-10-19
Freeman Pancreatic Flexi-Stent labeled with incorrect expiration dates
Hobbs Medical is recalling Freeman Pancreatic Flexi-Stents with incorrect expiration dates on device labels that extend shelf life. Devices were distributed in the US and internationally from March 2018 to September 2020.
Product
Freeman Pancreatic Flexi-Stent Catalog Number: 6548
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-0024-2023·2022-10-19
Hobbs Posi-Stop Injection Needles Recalled for Incorrect Expiration Date Labeling
Hobbs Medical, Inc. is recalling Posi-Stop Injection Needles with lot numbers ending in 'R' due to incorrect expiration dates on device labels. The mislabeling extends the apparent shelf life, potentially allowing use of expired sterile devices.
Product
Hobbs Posi-Stop Injection Needle Catalog Number: 4720
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0013-2023·2022-10-19
Hobbs Medical Cytology Brush Recalled for Incorrect Expiration Dates
Hobbs Medical is recalling its Cytology Brush (catalog 4204) because device labels show incorrect expiration dates that extend the claimed shelf life. Affected devices were distributed in the US and several other countries from March 2018 to September 2020.
Product
Hobbs Medical Cytology Brush Catalog Number: 4204
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
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-0064-2023·2022-10-19
Freeman Pancreatic Flexi-Stent recalled for incorrect expiration date
Hobbs Medical is recalling Freeman Pancreatic Flexi-Stent devices with incorrect expiration dates on labels that extend perceived shelf life beyond actual device longevity.
Product
Freeman Pancreatic Flexi-Stent Catalog Number: 6582
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-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-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-0019-2023·2022-10-19
Hobbs Scope Introducer Recalled for Incorrect Label Expiration Date
Hobbs Medical is recalling 140 units of its Hobbs Scope Introducer due to incorrect label expiration dates that extend the shelf life. Affected devices were distributed in the US and internationally from March 2018 to September 2020.
Product
Hobbs Scope Introducer Catalog Number: 4650
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-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
HighFDA (Devices)·Z-0045-2023·2022-10-19
Hobbs Biliary Pigtail Stent Kits Recalled Due to Incorrect Expiration Date Label
Hobbs Medical is recalling Biliary Pigtail Stent Kits distributed from March 2018 to September 2020 due to incorrect expiration date labels that extend the shelf life beyond the actual safe period.
Product
Hobbs Biliary Pigtail Stent Kits Catalog Number: 6108
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 (Food)·F-0033-2023·2022-10-19
Eden Organic Apple Juice Recalled for Excessive Patulin
Eden Foods is recalling Eden Organic Apple Juice in multiple sizes because excessive levels of patulin, a mycotoxin from rotted apples, were found in certain lots. Rotted apples were not removed during processing.
Product
Eden Organic Apple Juice in 32floz., 64floz., and 1.82L sizes, all sizes in glass bottle. Glass bottles packed 12, 32floz. bottles per wholesale case and 6, 64floz. / 1.82L bottles per wholesale case. 32floz. UPC code: 0 0024182 00067 2 32floz. GTIN case code: 1 0024182 00067 9
Category
Food
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-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-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-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-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