FDA Device Intelligence
Home › STANDARD TEXTILE CO., INC. › OR TOWEL PERVAL

OR TOWEL PERVAL

STANDARD TEXTILE CO., INC. · Model 48810423 · UDI-DI 00634916015997

FRL
10
510(k) clearances
209
Adverse events (1 deaths)
6
Recalls
391
Facilities

Description

OR TOWEL PERVAL GQT 18X31 JADE VAT DYED SURGICAL HMD 3-4 SIDE

Recalls

DateFirmReason
2021-05-25Medline Industries IncPotential for mold contamination (Aspergillus vadensis)
2017-12-11Medical Action Industries IncProduct sterility potentially compromised.
2016-03-31American Surgical CompanyProduct packaging defective compromising sterility
2016-03-31American Surgical CompanyProduct packaging defective compromising sterility
2009-07-21Coloplast Corp Skin Care DivColoplast determined that a portion of one lot of InterDry" Ag Lot number 1789435, did not meet the product specification for silver content. In this portion of the lot antimicrob
2006-02-093M Company / Medical DivisionAfter reviewing manufacturing records it has been determined that these lots inadvertently were not sterilized after packaging in individual boxes labeled as sterile product.

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.