---
title: "Parietex Composite Mesh Polyester with Absorbable Collagen Film, Horseshoe- S... — FDA record Z-1183-2023 | Is It on Recall"
description: "Collagen film was placed on the opposite side of the mesh may cause delay to treatment/therapy, adhesions, erosion/migration, pain, fistula, hernia (recurrence)"
url: https://isitonrecall.com/recall/fda-device-z-1183-2023-parietex-composite-mesh-polyester-with-absorbable-collagen-film-horseshoe-shaped-9-x-8-cm-3-6-x-3-1/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Parietex Composite Mesh Polyester with Absorbable Collagen Film, Horseshoe- Shaped, 9 x 8 cm (3.6" x 3.1"). Intended ... — FDA record Z-1183-2023

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 Jan 11, 2023. 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**: Parietex Composite Mesh Polyester with Absorbable Collagen Film, Horseshoe- Shaped, 9 x 8 cm (3.6" x 3.1"). Intended for the reinforcement of tissues during surgical repair Model Number: PCO2H3
- **Reason**: Collagen film was placed on the opposite side of the mesh may cause delay to treatment/therapy, adhesions, erosion/migration, pain, fistula, hernia (recurrence), and failure of implant
- **Classification**: Class II
- **Recalling firm**: Covidien, LP
- **Quantity**: 53 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1183-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1183-2023%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: A8845211784602 Lot Number: PVE0194M |

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

## Distribution

US Distribution to states of: CA, GA, NY and OUS Foreign distribution to countries of: Armenia, Belgium, France, Germany, Israel, Japan, Luxembourg, Romania, Spain, Switzerland and United Kingdom.

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

- [California](https://isitonrecall.com/state/california/)
- [Georgia](https://isitonrecall.com/state/georgia/)
- [New York](https://isitonrecall.com/state/new-york/)

## Dates in the source

- **Report date**: Mar 8, 2023
- **Recall initiation date**: Jan 11, 2023
- **Center classification date**: Feb 26, 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-1183-2023%22)

## Related records

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