Data Foundry

Medical device recalls 2017

Burn Sheet — Class II medical device recall Z-3078-2017

Terminated recall by Certified Safety Mfg Inc, reported 2017-09-06, distributed nationwide. Burn Sheet has possibility of being shredded.

Recall numberZ-3078-2017
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmCertified Safety Mfg Inc, Kansas City, MO, United States
Recall initiated2017-06-26
Classified2017-08-25
Reported by FDA2017-09-06
Terminated2020-11-03
DistributedNationwide (US)
Lot numbersJT09113, JT17513, JT36112
Model numbers30-01, 36M, 7305, K608-061, R505-091

Product

Burn Sheet, sterile - 60" x 96". Included in First Aid Kits: 36M - Delmarva Power/ACE - w/Logo, Certified Safety Manufacturing logo, and sold blank. product Usage: Provides sterile environment to protect patient from infection

Reason for recall

Burn Sheet has possibility of being shredded.

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-3078-2017. 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.