The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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9201–9225 of 27393

  • 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-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-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-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-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-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-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-0047-2023·2022-10-19

    Freeman Pancreatic Flexi-Stent Kit Recall: Incorrect Expiration Date Label

    Hobbs Medical is recalling Freeman Pancreatic Flexi-Stent Kits with incorrect expiration dates on labels, potentially allowing devices to be used beyond their actual safe shelf life. Affected units were distributed from March 2018 to September 2020.

    Product
    Freeman Pancreatic Flexi-Stent Kit Catalog Number: 6351
    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-0088-2023·2022-10-19

    Medline Venclose cardiovascular procedure kits recalled for wrong component size

    Medline Industries is recalling 1,760 Venclose procedure packs due to incorrect introducer/sheath component size. Affected kits contain 12cm components instead of the required 7cm.

    Product
    VENCLOSE, VENCLOSE PROCEDURE PACK, 7VM, REF VC-PPH-67A. Cardiovascular procedure convenience kit.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-0079-2023·2022-10-19

    Scalpel Handle Recall: Hu-Friedy K360 Separates and Poses Choking Risk

    Hu-Friedy K360 scalpel handles may separate from the grip during use, allowing the tip to fall into a patient's mouth and cause cuts or choking.

    Product
    Hu-Friedy K360 Scalpel Handle, 360 Degree Scalpel Handle, REF K360
    Category
    Medical Device
    Distribution
    5 states
  • 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-0086-2023·2022-10-19

    Veritas Advanced Infusion Packs Recalled for Broken Irrigation Luer

    Johnson & Johnson Surgical Vision is recalling 53,624 units of Veritas Advanced Infusion Packs due to manufacturing defects causing broken or cracked irrigation luers that could compromise ophthalmic surgical procedures.

    Product
    Veritas Advanced Infusion Packs. Used in ophthalmic procedures.
    Category
    Medical Device
    Distribution
    25 states
  • 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-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-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-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-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-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-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-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-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-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-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-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