---
title: "SUR-FIT Natura S4S Durahesive Wafer 70MM (1X10PK) US. Each market unit contai... — FDA record Z-1134-2022 | Is It on Recall"
description: "Firm received 10 complaints of skin barrier delamination issues (e.g. flange lifts from wafer, skin barrier layers separate) or tape border rips/tears."
url: https://isitonrecall.com/recall/fda-device-z-1134-2022-sur-fit-natura-s4s-durahesive-wafer-70mm-1x10pk-us-each-market-unit-contains-10-individual-wafers/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# SUR-FIT Natura S4S Durahesive Wafer 70MM (1X10PK) US. Each market unit contains 10 individual wafers. — FDA record Z-1134-2022

Reported terminated

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 Apr 22, 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**: SUR-FIT Natura S4S Durahesive Wafer 70MM (1X10PK) US. Each market unit contains 10 individual wafers.
- **Reason**: Firm received 10 complaints of skin barrier delamination issues (e.g. flange lifts from wafer, skin barrier layers separate) or tape border rips/tears.
- **Classification**: Class II
- **Recalling firm**: ConvaTec, Inc
- **Quantity**: 600 market units
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-1134-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1134-2022%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 | Product order number: ICC 413157; LOT Number 1H02899; Expiration Date: Aug 2026; DI Number: 00768455106189 |

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

## Distribution

Distributed nationwide to NJ, PA, OH, CA, AL, MI, NY, TX, FL, NC, VA, LA, IL, DE, KY, WA, KS, MN, MS and internationally to India.

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

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- [Georgia](https://isitonrecall.com/state/georgia/)
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- [Illinois](https://isitonrecall.com/state/illinois/)
- [Indiana](https://isitonrecall.com/state/indiana/)
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- [New York](https://isitonrecall.com/state/new-york/)
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- [Oklahoma](https://isitonrecall.com/state/oklahoma/)
- [Oregon](https://isitonrecall.com/state/oregon/)
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- [Utah](https://isitonrecall.com/state/utah/)
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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Jun 1, 2022
- **Recall initiation date**: Apr 22, 2022
- **Center classification date**: May 25, 2022
- **Termination date**: Mar 4, 2026

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-1134-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [ConvaTec, Inc records](https://isitonrecall.com/brand/convatec-inc/)
