LifeShield LATEX-FREE HemoSet 100 mL Burette I — Class II medical device recall Z-1479-2014
Terminated recall by Hospira Inc., reported 2014-04-30, distributed in FL, IA, IN, KS, KY, ME, MO, MT…. Hospira identified an incorrect lower lid (set component) had been supplied and was being used during the manu
| Recall number | Z-1479-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hospira Inc., Lake Forest, IL, United States |
| Recall initiated | 2014-02-25 |
| Classified | 2014-04-21 |
| Reported by FDA | 2014-04-30 |
| Terminated | 2016-11-28 |
| Distributed | FL, IA, IN, KS, KY, ME, MO, MT, PA, TN, TX, UT, VA, WA |
| Quantity | 3,893 sets |
| Lot numbers | 280055H, 341005H |
Product
LifeShield LATEX-FREE HemoSet 100 mL Burette I.V. PlumSet, Nonvented, 105 inch with Prepierced Reseals, OPTION-LOK and Inline Dual Channel Cassette. For administration of blood and blood bags for use with Plum Series Infusers.
Reason for recall
Hospira identified an incorrect lower lid (set component) had been supplied and was being used during the manufacturing process of list number 11241-03, a HemoSet containing a burette and blood filter, intended for infusion of blood/blood products. In a gravity delivery, the correct lower lid dispenses 15 drops per mL and the incorrect lower lid found dispenses 10 drops per mL.
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-1479-2014. 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.