Sheridan SHER-I-SLIP and SOFT-TIP Intubating Stylets are intubating… — Class II medical device recall Z-2587-2017
Ongoing recall by Teleflex Medical, reported 2017-06-21, distributed nationwide. Product size listed on the labeling is incorrect.
| Recall number | Z-2587-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Teleflex Medical, Research Triangle Park, NC, United States |
| Recall initiated | 2017-05-11 |
| Classified | 2017-06-14 |
| Reported by FDA | 2017-06-21 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, CZ, DE, DK, IL, PT |
| Quantity | 21,690 eaches |
| Reason classes | labeling |
| Lot numbers | 73A1700733, 73J1600218, 73K1600376, 73K1600587, 73L1600158, 73M1600275 |
Product
Sheridan SHER-I-SLIP and SOFT-TIP Intubating Stylets are intubating stylets manufactured from galvanized carbon steel and aluminum rods that are coated with a blue PVC or polypropylene outer covering and are designed to be placed inside an endotracheal tube to obtain a desired shape during intubation.
Reason for recall
Product size listed on the labeling is incorrect.
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-2587-2017. 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.