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GERSON

LOUIS M. GERSON CO. · Model 1730 · UDI-DI 00044585917308

MSH
1
510(k) clearances
194
Adverse events
3
Recalls
226
Facilities

Description

1730 Type N95 Particulate Respirator and Surgical Respirator

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

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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.