FDA Device recall Z-2601-2018
Polysorb Braided Absorbable Suture 1 36" 90 cm Undyed GS-21, Product Number CL-955
- FDA Device
- Class II
- terminated
- Published 2018-08-08
On 2018-08-08 the FDA classified a Class II recall of Polysorb Braided Absorbable Suture 1 36" 90 cm Undyed GS-21, Product Number CL-955 by Covidien, citing potential proplylene glycol contamination.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2601-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-06-15 |
| Published | 2018-08-08 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Covidien |
| Distribution | CA, NY, TX |
Product
Polysorb Braided Absorbable Suture 1 36" 90 cm Undyed GS-21, Product Number CL-955
Reason
Potential proplylene glycol contamination
Identifiers
| code_info | UDI - 10884521043718 /20884521043715 Lot Number - A8C0783X |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2601-2018%22
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