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143 Microfiber Shades

SIGVARIS INC · Model 143C · UDI-DI 00745129232382

HQL
5
510(k) clearances
76,239
Adverse events (4 deaths)
75
Recalls
57
Facilities

Description

A tube-like garment made of elastic material(e.g., circular knit nylon and spandex yarns) that exerts a pressure upon the limb upon which it is fitted (typically a leg, but some types may be used on an arm), primarily to improve venous return to treat/prevent one or more disorders of circulation(e.g. oedema, deep vein thrombosis (DVT), varicosis). It might be referred to as a compression stocking or flight sock and may be intended to apply a graduated pressure across a limb,however it is not intended to support an injured joint. It is normally available (non-prescription) over-the-counter (OTC) for home-use and/or for hospitalized or institutionalized patients. This is a reusable device.

Recalls

DateFirmReason
2026-02-19AMO Puerto Rico Manufacturing, Inc.Due to identifying a limited quantity of intraocular lenses that may have a haptic that sticks to the optic which prevents the lens from unfolding as consistently as expected.
2025-06-06Bausch & Lomb Surgical, Inc.An off-power error was identified, which resulted in a diopter of 16, rather than the intended 3 diopter. Implantation of affected intraocular lens could result in functional visua
2025-03-27Bausch & Lomb Surgical, Inc.In response to an increased number of reports of toxic anterior segment syndrome (TASS) in conjunction with implantation of enVista Aspire and enVista Envy IOLs, and certain enVist
2023-07-06Johnson & Johnson Surgical Vision, Inc.Their is a potential that intraocular lenses (IOLs) were manufactured with unintended toric fiducial marks.
2022-05-13Rayner Intraocular Lenses LtdThe outer package is mislabeled and the package contains a different IOL strength.
2022-05-11Alcon Laboratories Ireland, LtdDue to device (preloaded intraocular lens) mislabeling, associated with partial mixing of product during overlapping manufacturing runs, and attributed to improper manufacturing li
2020-06-09Bausch & Lomb Surgical, Inc.The toric axis marks were misaligned (from the expected position in relation to the haptics) on an implanted lens.
2020-04-17Alcon Research LLCIncorrect IOL diopter
2018-11-09Tekia, Inc.A limited number of lenses may be mislabeled with the incorrect diopter power.
2018-11-05Bausch & Lomb Surgical, Inc.Cosmetic imperfections on the surface of some lenses.

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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.