---
title: "Surgilon Braided Nylon suture Product Description: 88861883-51 SURGILON* 2-0 ... — FDA record Z-1178-2023 | Is It on Recall"
description: "Sterile Barrier Breach of Breather Pouch may cause infection or vision loss for ophthalmic procedures in cases where there is direct patient contact"
url: https://isitonrecall.com/recall/fda-device-z-1178-2023-surgilon-braided-nylon-suture-product-description-88861883-51-surgilon-2-0-blk-75cm-c16-88861915-71/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Surgilon Braided Nylon suture Product Description: 88861883-51 SURGILON\* 2-0 BLK 75CM C16 88861915-71 SURGILON\* 1 BLK... — FDA record Z-1178-2023

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Dec 2, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Surgilon Braided Nylon suture Product Description: 88861883-51 SURGILON\* 2-0 BLK 75CM C16 88861915-71 SURGILON\* 1 BLK 75CM GS11 88861919-31 SURGILON\* 4-0 BLK 7X75CMPCT 88861919-41 SURGILON\* 3-0 BLK 7X75CMPCT 88861919-51 SURGILON\* 2-0 BLK 7X75CMPCT 88861919-61 SURGILON\* 0 BLK 7X75CM PCT 88861919-71 SURGILON\* 1 BLK 7X75CM PCT 88861932-51 SURGILON\* 2-0 BLK 75CM GS10 88861971-71 SURGILON\* 1 BLK 75CM GS21 88861985-71 SURGILON\* 1 BLK 75CM SC1X36 SBS-1884G SURGILON\* 4-0 WHI 45CM P12X12 SBS-1928G SURGILON\* 5-0 BLK 45CM P13X12
- **Reason**: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss for ophthalmic procedures in cases where there is direct patient contact
- **Classification**: Class II
- **Recalling firm**: Covidien, LP
- **Quantity**: 87708 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1178-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1178-2023%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | GTIN: 20884521073996, 20884521076652, 10884521072183, 20884521072180, 10884521071223, 20884521071220, 10884521071797, 20884521071794, 20884521071763, 20884521071787, 20884521071749, 10884521073838, 20884521073835, 20884521076669, 10884521076662, 10884521071766, 20884521071725, 10884521071513, 20884521071510. Model Number Lot # 8886188351 D1K1677FY 8886191571 D2C3242Y 8886191931 D2B2243Y 8886191941 D1M2553Y D1M2561Y D2B0169Y 8886191951 D1M0915Y D2A0560Y D2B1245Y D2B1537Y D2B2751Y D2C0267Y D2C0907Y D2C1101Y D2D2347Y D2D2437Y D2D2506Y D2D2510Y D2E0905Y 8886191961 D1M1423Y D2A0861Y D2A0865Y D2A1709Y D2B1349Y D2B1350Y D2B2727Y 8886191971 D1M0640Y D1M1494Y D2C0962Y 8886193251 D1G1867Y 8886197171 D2B0290Y D2B0445Y D2B0476Y 8886198571 D1E0626Y SBS1884G D1E1212FY SBS1928G D2B0707FY D2C3247FY |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US Nationwide Distribution and OUS Foreign distribution to countries of: Albania Argentina Armenia Australia Austria Azerbaijan Belarus Belgium Bosnia And Herzegovina Brazil Bulgaria Cambodia Cameroon Canada Canary Islands Chile China Colombia Croatia Czech Republic Denmark Egypt Finland France Georgia Germany Ghana Greece Hong Kong Hungary India Indonesia Iran Iraq Ireland Israel Italy JAPAN Jordan Kazakhstan Kenya Korea, Republic Of Kosovo Kuwait Latvia Lebanon Lithuania Macao Malaysia Malta Mauritius Mexico Moldova, Republic Of Morocco Myanmar Namibia Netherlands New Zealand North Macedonia Norway Pakistan Panama Paraguay Philippines Poland Portugal Reunion Romania Russian Federation Saudi Arabia Serbia Singapore Slovakia Slovenia South Africa Spain Sweden Switzerland Syrian Arab Republic Taiwan Thailand Tunisia Turkey Uganda Ukraine United Arab Emirates United Kingdom Uruguay Uzbekistan Viet Nam Zimbabwe

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Alaska](https://isitonrecall.com/state/alaska/)
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- [North Dakota](https://isitonrecall.com/state/north-dakota/)
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- [Ohio](https://isitonrecall.com/state/ohio/)
- [Oklahoma](https://isitonrecall.com/state/oklahoma/)
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- [Rhode Island](https://isitonrecall.com/state/rhode-island/)
- [South Carolina](https://isitonrecall.com/state/south-carolina/)
- [South Dakota](https://isitonrecall.com/state/south-dakota/)
- [Tennessee](https://isitonrecall.com/state/tennessee/)
- [Texas](https://isitonrecall.com/state/texas/)
- [Utah](https://isitonrecall.com/state/utah/)
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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Mar 8, 2023
- **Recall initiation date**: Dec 2, 2022
- **Center classification date**: Feb 25, 2023

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1178-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Covidien, LP records](https://isitonrecall.com/brand/covidien-lp/)
