FDA Medical Device Recalls (openFDA)
Hobbs Medical, Inc.: Hobbs Medical 3 Prong Looped Retriever, a disposable device to be used by physician to remove foreign object or cauterize polyp specimens from the GI tract. REF: 5030 and 5030S
- Recall number
- Z-0824-06
- Recalling firm
- Hobbs Medical, Inc.
- Product
- Hobbs Medical 3 Prong Looped Retriever, a disposable device to be used by physician to remove foreign object or cauterize polyp specimens from the GI tract. REF: 5030 and 5030S
- Status
- Terminated
- Initiated
- 2006-03-15
- Posted
- 2006-05-03
- Terminated
- 2006-06-27
- Reason
- Diameter of device at the distal end would prevent it from passing through the endoscope's working channel.
- Root cause
- Process control
- Action
- Hobbs Medical notfied customers by Registered Letter on 3/15/06, requesting return of recalled product.
- Quantity
- 254 units
- Distribution
- AK, IA, KY, MI, NH, NC,UT, WI, Canada, and UK
- Lot, serial or model codes
- Lot Numbers: H11-05-040; H11-05-138; H11-05-139; H11-05-140;H11-05-141; H11-05-205.
- 510(k) numbers
- ["K833125"]
- PMA numbers
- not on file
- Product code
- KOG
- Firm FEI
- 1220592
- Firm city
- Stafford Springs
- Firm state
- CT
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28