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FDA Medical Device Recalls (openFDA)

Hobbs Medical, Inc.: Hobbs Medical Polypectomy Snare, Catalog No. 7202

Recall number
Z-1388-2022
Recalling firm
Hobbs Medical, Inc.
Product
Hobbs Medical Polypectomy Snare, Catalog No. 7202
Status
Open, Classified
Initiated
2022-06-03
Posted
not on file
Terminated
not on file
Reason
During use, the sheath of the device may accordion at the proximal end where the sheath meets the shrink band. Kinking of the sheath may prevent the snare from fully closing, and injury may result.
Root cause
Component design/selection
Action
On June 3, 2022, the firm distributed Urgent Medical Device Recall letters to affected customers. Customers were instructed to immediately cease use of the affected product and to return the product to Hobbs Medical. For questions related to the Acknowledgement Form and its return, please contact Hobbs Customer Service at 1-800-344-6227
Quantity
45 (US)
Distribution
Domestic distribution to NC, TX, and WA. Foreign distribution to Canada.
Lot, serial or model codes
UDI-DI: M84972020 Package UDI: M84972021 Lots: H11-20-017 H04-20-062 H04-19-056 H11-19-077 H08-17-014R H10-17-089R H10-17-089 H0S-17-014 H06-17-167
510(k) numbers
["K844074"]
PMA numbers
not on file
Product code
OCZ
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
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

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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

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