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-0058-2023·2022-10-19
Freeman Pancreatic Flexi-Stent Distributed with Incorrect Expiration Date
Hobbs Medical is recalling Freeman Pancreatic Flexi-Stent devices due to incorrect expiration dates on the device labels. Affected units distributed in the US and internationally from March 2018 to September 2020 may have been used beyond their actual safe shelf life.
Product
Freeman Pancreatic Flexi-Stent Catalog Number: 6544
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0043-2023·2022-10-19
Hobbs Biliary Pigtail Stent Kits Recalled for Incorrect Expiration Dates
Hobbs Medical is recalling Biliary Pigtail Stent Kits due to incorrect expiration dates on device labels that extend shelf life, affecting 15 units distributed from March 2018 to September 2020.
Product
Hobbs Biliary Pigtail Stent Kits Catalog Number: 6104
Category
Medical Device
Distribution
Distributed nationwide
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-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-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-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-0055-2023·2022-10-19
Freeman Pancreatic Flexi-Stent Recalled for Incorrect Expiration Date
Hobbs Medical recalled Freeman Pancreatic Flexi-Stents due to incorrect expiration dates on device labels. The mislabeled dates extend shelf life, potentially allowing use of expired devices.
Product
Freeman Pancreatic Flexi-Stent Catalog Number: 6533
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-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
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-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-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-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
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-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-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-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-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-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
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