Data Foundry

Medical device recalls 2022

Outer Packaging Label: Protekt Sharps Safety Knives — Class II medical device recall Z-1120-2022

Completed recall by International Science & Technology, LP, DBA Diamatrix Ltd., reported 2022-06-01, distributed nationwide. Surgical knives may contain incorrect description printed on handles. Specifically, some surgical knife handle

Recall numberZ-1120-2022
Product typeMedical device
ClassificationClass II
StatusCompleted
Voluntary or mandatedVoluntary
Recalling firmInternational Science & Technology, LP, DBA Diamatrix Ltd., Spring, TX, United States
Recall initiated2022-02-24
Classified2022-05-20
Reported by FDA2022-06-01
DistributedNationwide (US)
Countries outside the USDE
Quantity90 units
Lot numbersB923LUC
Model numbers2.2MM, 44620MU

Product

Outer Packaging Label: Protekt Sharps Safety Knives - REF: PG 44620MU, Sterile R, Multi-Use 2.2mm Double Bevel Slit, Angled 6 units, Individual Packaging Label: ProTekt Sharps Safety Knives - REF: PG 44620MU,2.2mm double Bevel Slit, Sterile R, Angled 1 unit, Handle Labeling; 2.5mm slit double bevel

Reason for recall

Surgical knives may contain incorrect description printed on handles. Specifically, some surgical knife handles may contain a size of "2.5mm" when the actual size is "2.2mm".

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-1120-2022. 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.