Hospira LifeShield Latex-Free 100 mL Burette Set — Class II medical device recall Z-2075-2012
Terminated recall by Hospira Inc., reported 2012-08-01, distributed nationwide. The float valve in the burette sticks to the burette wall and does not open or close properly.
| Recall number | Z-2075-2012 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hospira Inc., Lake Forest, IL, United States |
| Recall initiated | 2012-07-13 |
| Classified | 2012-07-25 |
| Reported by FDA | 2012-08-01 |
| Terminated | 2016-11-28 |
| Distributed | Nationwide (US) |
| Countries outside the US | BB, CA |
| Quantity | 4,420 sets |
| Lot numbers | 96-098-5H |
Product
Hospira LifeShield Latex-Free 100 mL Burette Set, Convertible Pin, 77 inch with 2 Prepierced Injection Sites and Option-Lok Microdrip Soluset with Calibrated Burette and Precision Drip Chamber; an Rx sterile medical device used to administer fluids; 20 individually wrapped sets per case; Made in Costa Rica, Hospira, Inc., Lake Forest, IL 60045 USA; list 12722-65. Intended use: for the administration of fluids.
Reason for recall
The float valve in the burette sticks to the burette wall and does not open or close properly.
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-2075-2012. 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.