Data Foundry

Medical device recalls 2012

Vital Signs Disposable General Purpose 9 French Temperature Probe For… — Class II medical device recall Z-0407-2013

Terminated recall by Vital Signs Colorado Inc., reported 2012-11-28, distributed nationwide. There is a potential for epistaxis during use of the Disposable General Purpose 9 French Temperature Probe.

Recall numberZ-0407-2013
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmVital Signs Colorado Inc., Englewood, CO, United States
Recall initiated2012-08-17
Classified2012-11-20
Reported by FDA2012-11-28
Terminated2013-06-14
DistributedNationwide (US)
Countries outside the USAU, CH, DE, GB, NL, NZ
Quantity243,685 units
Lot numbers12089A, 12090B, 12100A, 12101B, 12102A, 12108B, 12109B, 12114B, 12117B, 12130B, 12131A, 12138A, 12157B, 12173A, 5573Q, 5574A, 5574B, 5574X, 5574Y, 5574Z, 5575A, 5578K, 5578L, 5580Y, 5580Z, 5581A, 5581L, 5583E, 5584C, 5584D, 5586X, 5603R, 5606U, 5614N, 5615N, 5621U, 5623H, 5631C, 5632V, 5633T and 32 more
Model numbers1016, 1016EU, R1016ES

Product

Vital Signs Disposable General Purpose 9 French Temperature Probe For monitoring of core temperature

Reason for recall

There is a potential for epistaxis during use of the Disposable General Purpose 9 French Temperature Probe.

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-0407-2013. 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.