Stryker recalls Spy-Phi Drape HH2020 Pack of 20 (sold internationally) due to sterile drapes packaged in unsealed pouches. Affected lots listed in record; no remedy specified.
Sterile drapes packaged in an unsealed pouch.
Stryker is recalling Spy-Phi Drape HH2020 packs of 20 sold internationally because they were packaged in unsealed pouches. This could lead to contamination of sterile drapes if not properly sealed.
Sterile drapes packaged in unsealed pouches may become contaminated during storage or handling. This could compromise the sterility of the drapes when used in medical procedures.
Healthcare professionals using these drapes in medical settings are most at risk. The recall applies to specific international lots sold between 2017 and 2019.
Check for the product name 'Spy-Phi Drape HH2020' and the lot numbers listed in the recall (e.g., 1703011, 1703021, etc.). These drapes were sold internationally between 2017 and 2019.
Look for the lot number on the drape packaging, which should match one of the listed numbers (e.g., 1703011, 1703021).
The sterile drapes were packaged in unsealed pouches, which could lead to contamination if not properly sealed.
Check the product name 'Spy-Phi Drape HH2020' and the lot number on the packaging; affected lots are listed in the recall record.
The recall record does not specify a remedy, so contact Stryker directly for guidance.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-1926-2020 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-1926-2020 from Stryker. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
