FDAMarch 16, 2017device

Vitrectomy Pack, part number AMS4952 Product packaged in a convenient manner for use in a general clinical procedure

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised.

What to do

FDA enforcement status: Terminated

Brands named

windstone medical packagingwindstonewindstone medical

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Vitrectomy Pack, part number AMS4952 Product packaged in a convenient manner for use in a general clinical procedure — Recall Details · AllClear