Data Foundry

Medical device recalls 2023

Ti-Cron Coated Braided Polyester Suture Product Description… — Class II medical device recall Z-1181-2023

Ongoing recall by Covidien, LP, reported 2023-03-08, distributed nationwide. Sterile Barrier Breach of Breather Pouch may cause infection or vision loss for ophthalmic procedures in cases

Recall numberZ-1181-2023
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmCovidien, LP, North Haven, CT, United States
Recall initiated2022-12-02
Classified2023-02-25
Reported by FDA2023-03-08
DistributedNationwide (US)
Countries outside the USAE, AR, AT, AU, BE, BG, BR, CA, CH, CL, CN, CO, CZ, DE, DK, EG, ES, FI, FR, GB, GH, GR, HK, HR, HU, ID, IE, IL, IN, IQ, IR, IT, JO, JP, KE, KR, KW, LB, LT, LV, MA, MT, MX, MY, NL, NO, NZ, PA, PH, PK, PL, PT, PY, RO, RS, SA, SE, SG, SI, SK, TH, TN, TR, TW, UA, UY, VN, ZA
Quantity40,152 units
Reason classessterility
UPC / GTIN / UDI-DI10884521058620, 10884521059290, 10884521059900, 10884521060432, 10884521061194, 10884521061293, 10884521061507, 10884521062320, 20884521058627, 20884521059006, 20884521059013, 20884521059020, 20884521059204, 20884521059280, 20884521059297, 20884521059372, 20884521059396, 20884521059464, 20884521059471, 20884521059570, 20884521059907, 20884521059990, 20884521060095, 20884521060101, 20884521060170 and 16 more
Lot numbers8886277531, 8886288041, 8886301261, 8886301561, 8886301751, 8886302671, 8886303551, 8886304741, 8886304851, 8886305061, 8886305451, 8886305689, 8886305953, 8886307051, 8886308851, 8886309051, 8886309271, 8886310943, 8886311179, 8886311961, 8886315409, 8886315931, 8886316041, 8886316361, 8886318541, 8886318641, 8886321251, 8886322641, 8886328021, 8886328031, 8886330971, 8886336931, 8886339351, CD3123K, D1D0290Y, D1D2540FY, D1D2597Y, D1D3149FY, D1D3218FY, D1E0506Y and 39 more
Model numbers8886277531, 8886288041, 8886301261, 8886301561, 8886301751, 8886302671, 8886303551, 8886304741, 8886304851, 8886305061, 8886305451, 8886305689, 8886305953, 8886307051, 8886308851, 8886309051, 8886309271, 8886310943, 8886311179, 8886311961, 8886315409, 8886315931, 8886316041, 8886316361, 8886318541 and 54 more

Product

Ti-Cron Coated Braided Polyester Suture Product Description 88862775-31 TICRON* 4-0 BLU 75CM CV327DA 88862880-41 TICRON* 3-0 WHI 75CM Y31DA 88863012-61 TICRON* 0 BLU 90CM C16 X36 88863015-61 TICRON* 0 BLU 120CM V20X36 88863017-51 TICRON* 2-0 BLU 120CM SKX36 88863026-71 TICRON* 1 BLU 75CM HOS12X36 88863035-51 TICRON 2-0 BLU 105CM CV305DA 88863047-41 TICRON* 3-0 BLU 45CM C13X36 88863048-51 TICRON* 2-0 BLU 75CM C13X36 88863050-61 TICRON* 0 BLU 75CM C14 X36 88863054-51 TICRON* 2-0 BLU 75CM C17X36 88863056-89 TICRON* 5 BLU 45CM GS18X12 88863059-53 TICRON* 2-0 BLU 45CM P24X12 88863070-51 TICRON* 2-0 BLU 75CM C15X36 88863088-51 TICRON* 2-0 BLU 75CM Y5X36 88863090-51 TICRON 2-0 BLU 75CM GS21X36 88863092-71 TICRON* 1 BLU 75CM KV37X36 88863109-43 TICRON* 3-0 BLU 45CM P22X12 88863111-79 TICRON* 5 BLU 75CM HGS21X36 88863119-61 TICRON* 0 BLU 75CM KV34X36 88863154-09 TICRON* 4 BLU 75CM GS11X36 88863159-31 TICRON* 4-0 BLU 90CM KV5DA 88863160-41 TICRON* 3-0 BLU 90CM Y31DA 88863163-61 TICRON* 0 BLU 75CM SC1 X36 88863185-41 TICRON* 3-0 BLU 75CM CV305 88863186-41 TICRON* 3-0 BLU 75CM CV331 88863212-51 TICRON* 2-0 BLU 90CM Y5DA7P 88863226-41 TICRON* 3-0 BLU 60CM CV330DA 88863280-21 TICRON* 5-0 BLU 75CM CV301DA 88863280-31 TICRON* 4-0 BLU 75CM CV301DA 88863309-71 TICRON* 1 BLU 75CM GS11X36 88863369-31 TICRON* 4-0 BLU 90CM CV316DA 88863393-51 TICRON* 2-0 BLU 90CM CV300DA CD-3123K TICRON* 5-0 WHI 45CM SS24 DA

Reason for recall

Sterile Barrier Breach of Breather Pouch may cause infection or vision loss for ophthalmic procedures in cases where there is direct patient contact

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-1181-2023. 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.