Pleur-Evac Adult-Ped Wet — Class II medical device recall Z-2749-2020
Terminated recall by TELEFLEX MEDICAL INC, reported 2020-08-12, distributed nationwide. Potential for sterile packaging to be compromised¿
| Recall number | Z-2749-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | TELEFLEX MEDICAL INC, Morrisville, NC, United States |
| Recall initiated | 2020-06-30 |
| Classified | 2020-08-03 |
| Reported by FDA | 2020-08-12 |
| Terminated | 2026-07-02 |
| Distributed | Nationwide (US) |
| Quantity | 1,812 units |
| Reason classes | sterility |
| Lot numbers | 74A1801125, 74A1902739, 74A2000267, 74A2000268, 74A2000745, 74A2000746, 74A2000747, 74A2001170, 74A2001171, 74A2001934, 74A2001935, 74A2001936, 74B1800758, 74B2000067, 74B2000068, 74B2000363, 74B2000364, 74C1800921, 74C1801541, 74C1900767, 74C1902202, 74C2000217, 74C2000474, 74C2001737, 74C2001769, 74C2001770, 74D1700243, 74D1801534, 74D1802402, 74D1902703, 74E1701799, 74E1900882, 74E1901526, 74F1500554, 74F1500555, 74F1500731, 74F1700647, 74F1700648, 74F1702092, 74F1900390 and 30 more |
Product
Pleur-Evac Adult-Ped Wet, LF Eng/Spanish, product code: A-8000I-06 - Product Usage: CHEST DRAINAGE: To evacuate air and/or fluid from the chest cavity or mediastinum. To help prevent air and/or fluid from re-accumulating in the chest cavity or mediastinum. To help re-establish and maintain normal intra-thoracic pressure gradients. To facilitate complete lung re-expansion to restore normal breathing dynamics.
Reason for recall
Potential for sterile packaging to be compromised¿
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-2749-2020. 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.