Data Foundry

Medical device recalls 2013

Dual Tip Marker — Class III medical device recall Z-1025-2013

Terminated recall by Viscot Medical LLC, reported 2013-04-10, distributed nationwide. Dual Tip Marker has inconsistent ink flow on the black permanent ink side.

Recall numberZ-1025-2013
Product typeMedical device
ClassificationClass III
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmViscot Medical LLC, East Hanover, NJ, United States
Recall initiated2012-08-22
Classified2013-03-29
Reported by FDA2013-04-10
Terminated2014-07-21
DistributedNationwide (US)
Quantity458,589 markers
Lot numbers022043, 022045, 022046, 042084, 042085, 042086, 042087, 042088, 042089, 052128, 052129, 052130, 052131, 062167, 062168, 062169, 062170, 072200, 072201, 072203, 072205, 072206, 072207

Product

Dual Tip Marker, Sterile Product Usage: A writing instrument intended to mark paper and plastic items around the sterile field during surgery. It has two tips. One is black for miscellaneous use. The other is for surgical skin marking.

Reason for recall

Dual Tip Marker has inconsistent ink flow on the black permanent ink side.

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-1025-2013. 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.