Data Foundry

Medical device recalls 2020

Spy-Phi Drape only — Class II medical device recall Z-1926-2020

Ongoing recall by Stryker Corporation, reported 2020-05-13, distributed nationwide. Sterile drapes packaged in an unsealed pouch.

Recall numberZ-1926-2020
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmStryker Corporation, San Jose, CA, United States
Recall initiated2020-01-07
Classified2020-05-07
Reported by FDA2020-05-13
DistributedNationwide (US)
Countries outside the USAT, AU, BE, CA, CH, CL, CN, CO, CZ, DE, DK, ES, FI, FR, GB, GR, HK, IE, IL, IN, IT, JP, KR, MY, NL, NZ, PH, PL, QA, RO, RU, SE, SG, TH, TR, TW, ZA
Quantity21,078 units
Reason classessterility
UPC / GTIN / UDI-DI20858701006326
Lot numbers1703011, 1703021, 1703031, 1703041, 1703051, 1703061, 1703071, 1703081, 1703091, 1703101, 1703111, 1703121, 1703131, 1703141, 1703151, 1703161, 1703171, 1703181, 1703191, 1703201, 1703211, 1703221, 1703231, 1703241, 1703251, 1703261, 1703271, 1703281, 1703291, 1703301, 1703311, 1704011, 1704021, 1704031, 1704041, 1704051, 1704061, 1704071, 1704081, 1704091 and 226 more

Product

Spy-Phi Drape only (HH2020) Pack of 20 HH2000 (Sold internationally only). Drape/ UDI: HH2020/20858701006326

Reason for recall

Sterile drapes packaged in an unsealed pouch.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1926-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.