AsthmaNefrin Starter Kit contains ten — Class I medical device recall Z-1372-2013
Terminated recall by Nephron Pharmaceuticals Corp., reported 2013-06-05, distributed nationwide. Possible dislodgement of the "Plate A", if this instance occurs, it presents a potential choking hazard.
| Recall number | Z-1372-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Nephron Pharmaceuticals Corp., Orlando, FL, United States |
| Recall initiated | 2013-04-30 |
| Classified | 2013-05-29 |
| Reported by FDA | 2013-06-05 |
| Terminated | 2016-06-28 |
| Distributed | Nationwide (US) |
| Countries outside the US | GB, GT, PA, PL |
| Quantity | 241,538 kits |
| Lot numbers | R2029A, R2029B, R2039A, R2042A, R2045A, R2047A |
Product
AsthmaNefrin Starter Kit contains ten (10) AsthmaNefrin vials and one (1) EZ Breathe Atomizer. For the delivery of liquid medications for respiratory usage.
Reason for recall
Possible dislodgement of the "Plate A", if this instance occurs, it presents a potential choking hazard.
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-1372-2013. 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.