# FDA recall Z-1134-2019

> **Ethicon, Inc.** · Class II · device recall initiated 2019-03-12.

## Product

VICRYL Sutures  VICRYL SUTURE 18"(45CM) 0 VIO  VICRYL SUTURE 18"(45CM) 4-0 UND  VICRYL SUTURE 18"(45CM) 2-0 VIO  VICRYL SUTURE 18"(45CM) 0 VIO  VICRYL SUTURE 18"(45CM) 2-0 VIO  VICRYL CT VIO 8X18IN 0 S/A CT-1 CR  VICRYL SUTURE 18"(45CM) 1 VIO  VCL CT UD 8X18IN 2-0 S/A CP-2 CR  VCL CT VIO 8X18IN 3-0 S/A SH-1 CR  VICRYL CT VIO 8X18IN 2-0 S/A SH CR  VICRYL CT UD 8X18IN 2-0 S/A CT-1 CR  VICRYL CT UD 8X18IN 0 S/A CT-1 CR   VCL CT UD 8X18IN 1 S/A CT-1 CR 9   VICRYL SUTURE 18"(45CM) 0 UND   VICRYL CT VIO 8X27IN 0 S/A CT-1 CR   VICRYL SUTURE 27"(70CM) 1 UND   VICRYL CT UD 8X27IN 0 S/A CT-1 CR   VICRYL SUTURE 27"(70CM) 0 VIO

## Reason for recall

VICRYL Suture, VICRYL Plus Suture, PDS Suture- may contain product that does not match the sales unit carton and foil label.

## Distribution

Worldwide distributions - US Nationwide and countries of   AUSTRALIA  BELGIUM  CANADA  CHINA  ISRAEL  JAPAN  PUERTO RICO  SINGAPORE

## Key facts

- **Recall number:** Z-1134-2019
- **Recalling firm:** Ethicon, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-03-12
- **Report date:** 2019-04-24
- **Termination date:** 2020-07-17

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Somerville, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1134-2019

## Citation

> AI Analytics. FDA recall Z-1134-2019. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1134-2019. Source: US FDA. Licensed CC0.

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