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Familex Face Mask
PHU BAO GROUP COMPANY LIMITED · Model Yellow · UDI-DI 08938504806090
10
510(k) clearances
127
Adverse events
9
Recalls
803
Facilities
Description
• 3 Ply - Disposable High Filtration Face Mask • Face Mask Size: 170mm x 90mm (± 5 mm) • Non - sterile, single use • Color Yellow • 50 masks pack in one box • Box dimensions: 185x105x90mm
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-05-18 | MEDLINE INDUSTRIES, LP - Northfield | Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams. |
| 2023-05-15 | MEDLINE INDUSTRIES, LP - Northfield | Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications. |
| 2021-01-07 | Cardinal Health 200, LLC | Gowns included in the kits potentially have rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns. |
| 2021-01-07 | Cardinal Health 200, LLC | Gowns included in the kits potentially have rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns. |
| 2021-01-07 | Cardinal Health 200, LLC | Gowns included in the kits potentially have rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns. |
| 2021-01-07 | Cardinal Health 200, LLC | Gowns included in the kits potentially have rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns. |
| 2021-01-07 | Cardinal Health 200, LLC | Gowns included in the kits potentially have rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns. |
| 2021-01-07 | Cardinal Health 200, LLC | Gowns included in the kits potentially have rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns. |
| 2017-09-11 | Zimmer Biomet, Inc. | Cut resistant surgical glove liners lack sterility assurance. |
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Get your free API keyRead the docsData 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.
