Data Foundry

Medical device recalls 2013

WASP — Class III medical device recall Z-2131-2013

Terminated recall by Copan Italia, reported 2013-09-11, distributed in CA, OR. The recall of the WASP (Walk Away Specimen Process) instrument was initiated because Copan Italia SpA has upgr

Recall numberZ-2131-2013
Product typeMedical device
ClassificationClass III
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmCopan Italia, Brescia, N/A, Italy
Recall initiated2013-08-09
Classified2013-08-30
Reported by FDA2013-09-11
Terminated2013-12-12
DistributedCA, OR
Countries outside the USBE, CA, CH, DE, DK, FI, FR, GB, IE, IT, JP, NO, RO, SE, ZA
Quantity63 units
Reason classessoftware
Serial numbers110, 111, 113, 124, 139, 147, 180, 187, W086-050-143/155, W086-050-164/169/159/175, W086-050-177/178/183, W086-050-179, W086-61-088/097/100/117, W086-61-093, W086-61-096, W086-61-103/137/141/142
Model numbersW086

Product

WASP (Walk Away Specimen Process). Automatic Planting and Streaking Instrument Catalog number: W086 WASP is a fully automated system used to process microbiological specimens in liquid phase for the investigation of infectious microbes.

Reason for recall

The recall of the WASP (Walk Away Specimen Process) instrument was initiated because Copan Italia SpA has upgraded the software concerning the broth inoculation table feature. The upgrade has been considered necessary from the manufacturer in order to eliminate the very low risk of rotation of the broth table when the door is open.

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-2131-2013. 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.