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Sklar Instruments: ECONO STERILE medical procedure kits

Reward FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer

Recall reason: Reports of various packaging issues that may result in a breach of the sterile barrier.. Recalled by Sklar Instruments. Distribution: Domestic: Nationwide Distribution. Classification (Class II — potential health risk). Affected lots/dates: 1) 94-0286, UDI/DI 50649111094406, Lot codes: FSF21; 2) 94-0290, UDI/DI 50649111095045, Lot codes: SK-115; 3) 94-029. Contact the manufacturer or the retailer where you purchased this device to arrange for a free correction, repair, or replacement.

Reward FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Category Product Recalls & Refunds
Location National
Eligibility U.S. consumers who own or purchased the recalled medical device. Contact the manufacturer or the retailer/pharmacy where you purchased it to arrange for a free correction, repair, or replacement. Have the model number ready if possible.
Source Official Source ↗
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