The Recall Desk

Manufacturer

Hobbs Medical, Inc.

72 recalls in our database name Hobbs Medical, Inc. as the manufacturing or recalling firm.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

51–72 of 72

  • HighFDA (Devices)·Z-0062-2023·2022-10-19

    Freeman Pancreatic Flexi-Stent recalled for incorrect expiration date labeling

    Hobbs Medical is recalling Freeman Pancreatic Flexi-Stent devices due to incorrect expiration dates on product labels. The labeling error extends the stated shelf life, potentially allowing use of degraded devices.

    Product
    Freeman Pancreatic Flexi-Stent Catalog Number: 6567
    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-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-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-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-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-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-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
  • 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-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-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-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-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-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-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
  • 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-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
  • HighFDA (Devices)·Z-1388-2022·2022-07-27

    Hobbs Medical Polypectomy Snare May Fail to Close Properly

    Hobbs Medical Polypectomy Snares (Catalog No. 7202) may accordion at the proximal end, preventing full closure and potentially causing injury. Specific lots distributed to medical facilities in NC, TX, WA, and Canada are affected.

    Product
    Hobbs Medical Polypectomy Snare, Catalog No. 7202
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0711-2022·2022-03-09

    Bronchial Microbiology Brush Labeling Error—Cleared Only for Gastrointestinal Use

    Hobbs Medical is recalling 38,357 Bronchial Microbiology Brushes due to labeling that incorrectly indicates bronchial use. The device is cleared only for gastrointestinal use.

    Product
    Bronchial Microbiology Brush, Catalog Number 4310 and 4320. Microbial sampling is performed by compressing a spring as the base of brush wire to expose the brush, scraping the desired surface, and releasing the compression on the spring which retracts the brush back into the shea
    Category
    Medical Device
    Distribution
    Distributed nationwide