Hobbs Medical, Inc. recalls
Every recall we track for Hobbs Medical, Inc. — 73 in all, from 2018–2024 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Hobbs Medical, Inc. dropped to zero in 2025 (0, down from 9 in 2024).
All FDA recall records for Hobbs Medical, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 1 | 0 | 1 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 1 | 0 | 1 |
| 2022 | 0 | 1 | 61 | 0 | 62 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 1 | 8 | 0 | 9 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Hobbs Medical, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Hobbs Medical, Inc. recalls
5 shown- Lower riskMedical device
Hobbs Medical, Inc. recalls Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4723
Hobbs Medical recalls Posi-Stop 25 Gauge needles (Catalog 4723) due to debris blocking flow. Affected units include specific lot numbers. Contact for return or replacement.
Hobbs MedicalOct 4, 2024 - Lower riskMedical device
Hobbs Medical, Inc. recalls Hobbs Medical Polypectomy Snare Catalog Number: 4575-OLY
Hobbs Medical recalls polypectomy snare devices with incorrect expiration dates extending shelf life. Affected units sold 3/25/2018-9/28/2020 with expiration dates up to 2025-09-01. No remedy specified in recall notice.
Hobbs MedicalJul 29, 2022 - Use cautionMedical device
Hobbs Medical, Inc. recalls Hobbs Medical Polypectomy Snare, Catalog No. 7202
Hobbs Medical recalls polypectomy snare (Catalog No. 7202) due to sheath kinking risk during use, which may cause injury. Affected units include specific lots and package UDI codes.
Hobbs MedicalJun 3, 2022 - Lower riskMedical device
Hobbs Medical, Inc. recalls Bronchial Microbiology Brush, Catalog Number 4310 and 4320. Microbial sampling is performed by compressing a spring as
Hobbs Medical recalls Bronchial Microbiology Brush models 4310 and 4320 due to incorrect labeling for bronchial use. These devices are cleared for gastrointestinal use only, not bronchial.
Hobbs MedicalDec 28, 2021 - Lower riskMedical device
Hobbs Medical, Inc. recalls Hobbs Bronchial Cytology Brushes, Model Number 4202; 4204; 4206 To be utilized by a trained physician and/or trained
Hobbs Medical recalls bronchial cytology brushes (models 4202, 4204, 4206) that were marketed for uses outside FDA clearance. These brushes are intended for trained medical professionals during endoscopic procedures.
Hobbs MedicalMay 1, 2018
Hobbs Medical, Inc. recall questions
How many recalls has Hobbs Medical, Inc. had?
73 recalls from Hobbs Medical, Inc. are on record with U.S. safety agencies, from 2018–2024.
What is the most recent Hobbs Medical, Inc. recall?
Hobbs Medical, Inc. recalls Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4723, dated Oct 4, 2024. Every Hobbs Medical, Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Hobbs Medical, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Hobbs Medical, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.