Hobbs Medical Polypectomy Snare recall
Hobbs Medical Polypectomy Snare, Catalog No. 7202
Why was Hobbs Medical Polypectomy Snare recalled?
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.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
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
- Product
- Hobbs Medical Polypectomy Snare, Catalog No. 7202
- Recalling firm
- Hobbs Medical, Inc.
- Quantity
- 45 (US)
- Distribution
- Domestic distribution to NC, TX, and WA. Foreign distribution to Canada.
- Recall date
- July 27, 2022
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)