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2-lumen Catheter for Cystometry and Urethral

Laborie Medical Technologies Canada ULC · Model 9021P5082 · UDI-DI 10627825008317

FEN
10
510(k) clearances
119
Adverse events (1 deaths)
3
Recalls
56
Facilities

Recalls

DateFirmReason
2019-07-17LABORIE MEDICAL TECHNOLOGIES, CORPPower supply unit (PS-SBL) not correctly labeled, and insulation material used at the low voltage DC end does not meet all applicable flammability rating requirements. may lead to
2018-07-03ConvaTec, IncBubble Leak Testing on AbViser AutoValve IAP Monitoring Devices without Transducer confirmed the potential for a pinhole breach in the sterile barrier.
2006-10-04Laborie Medical TechnologiesMislabeling: Product labeled with incorrect "Use Before" date and pouch labels missing lot number. (Incorrect dates-2006/07 or 2006/08; correct Use by dates-2009/08 for Lot 36H03M

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.