Data Foundry

Medical device recalls 2019

Stryker Sustainability Solutions — Class II medical device recall Z-0973-2019

Terminated recall by Stryker Sustainability Solutions, reported 2019-03-13, distributed nationwide. Affected lots of reprocessed arthroscopic shavers may display the incorrect catalog number and speed settings

Recall numberZ-0973-2019
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmStryker Sustainability Solutions, Tempe, AZ, United States
Recall initiated2018-07-27
Classified2019-03-05
Reported by FDA2019-03-13
Terminated2020-09-17
DistributedNationwide (US)
Countries outside the USCA, IL
Quantity14,265 units
Model numbers375-450-000, 375-532-000, 375-534-000, 375-542-000, 375-544-000, 375-545-000, 375-548-000, 375-552-000, 375-554-000, 375-555-000, 375-562-000, 375-564-000, 375-565-000, 375-747-000, 375-940-000, 375-940-012, 375-941-000, 375-941-012, 375-941-500, 375-950-000, 375-950-012, 375-950-112, 375-951-000, 375-951-012, 375-951-100 and 276 more

Product

Stryker Sustainability Solutions (SSS) reprocessed Arthroscopic Shavers Arthroscopic shavers can be used to abrade, cut and excise tissue and bone; remove loose fragments; and, shave away debris in arthroscopic surgeries, as well as surgeries of the jaw and sinuses. Intended for use in orthopedic surgical procedures of the joints, jaw or sinuses where the cutting and removal of soft and hard tissue or bone is needed in patients requiring orthopedic surgery.

Reason for recall

Affected lots of reprocessed arthroscopic shavers may display the incorrect catalog number and speed settings when connected to the generator, require manual mode for use on CORE generators, or display an error message on Crossfire 1 and 2 generators which does not allow the device to be used.

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-0973-2019. 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.