PFM Medical Multi-Snare Set
PFM Medical is recalling Multi-Snare Set catheter devices due to a failure to meet biocompatibility requirements for in-vitro cytotoxicity.
Stop using the affected devices immediately and contact the manufacturer for return instructions.
Why it was recalled
PFM Medical is recalling Multi-Snare Set catheter devices due to a failure to meet biocompatibility requirements for in-vitro cytotoxicity. Use of these devices in the vascular system may cause localized inflammation and tissue irritation.
Is mine affected?
Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.
Multi-Snare Set: 5 mm x 125 cm, REF: 147305; 10 mm x 125 cm, REF: 147310
- Lot code
- 147305, 1049868, 2028
- UDI-DI
- 04042301061829, 04042301033567
Where it was sold
Distributed nationwide.
Timeline
- Firm initiated recall
- Publicly announced
- Listed on Recall Canary
- Summary updated
Official source
Other Device Defect recalls
Editorial summary by Recall Canary · summary updated 2026-06-24 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification