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Home Health US, Incorporated: One Step Sterile Lancet for Single Use (3 sizes):

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

Recall reason: Due to incorrect/lack of Unique Device Identifier (UDI) codes.. Recalled by Home Health US, Incorporated. Distribution: U.S.: Nation-wide distributed thru Amazon U.S. States include: AZ, CA, FL, IL, NC, NM, NY, TN, TX, and VA. O.U.S.: N/A. Classification (Class III — minor violation). Affected lots/dates: UDI-DI code / Size: 06949517008861 / 30g Lot Number: 2312290802 06949517008854 / 28g Lot Number: 2406310201 069495170. 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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