FDA Device Intelligence
HomeBOUND TREE MEDICAL, LLC › Curaplex

Curaplex

BOUND TREE MEDICAL, LLC · Model 670245-KIT · UDI-DI 00810071633102

MSH
10
510(k) clearances
194
Adverse events
3
Recalls
226
Facilities

Description

Curaplex N95 Mask Kit (20 Masks)

Recalls

DateFirmReason
2023-08-09O&M HALYARD, INC.One respirator sample failed a filtration efficiency test. This respirator may not provide adequate protection to the user.
2008-07-23Inovel LLCDisplay boxes labeled as FRN95-MLEZ, Medium/Large Size Respirators were inadvertently mixed with Display Boxes labeled for FRN95-SEZ Small Size Respirators.
2006-02-20Inovel LLCMislabeling-A customer reported mislabeled product display boxes. Review of complaint samples and inventory confirmed that some product display boxes are labeled with incorrect mod

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
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.