Data Foundry

Medical device recalls 2023

Surgipro Monofilament Polypropylene Sutures Product Description… — Class II medical device recall Z-1179-2023

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-1179-2023
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
Quantity8,604 units
Reason classessterility
UPC / GTIN / UDI-DI20884521036519, 20884521036540, 20884521037868, 20884523004387
Lot numbersCP535, CP824, CP825, D2B1270Y, D2C1521Y, D2C3234Y, D2D0251Y, D2D1493Y, D2E1342Y, D2E1389Y, D2E1580Y, D2E2678Y, D2E2679Y, D2F0509Y, VP543
Model numbersCP535, CP824, CP825, D2B1270Y, D2C1521Y, D2C3234Y, D2D0251Y, D2D1493Y, D2E1342Y, D2E1389Y, D2E1580Y, D2E2678Y, D2E2679Y, D2F0509Y, VP543

Product

Surgipro Monofilament Polypropylene Sutures Product Description CP-535 SURGIPRO* 1 BLU 100CM GS24 X36 CP-824 SURGIPRO* 1 BLU 150CM GS26 X24 CP-825 SURGIPRO* 2 BLU 150CM GS26 X24 VP-543 SURGIPRO* 2-0 BLU 120CM V20 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-1179-2023. 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.