---
title: "TRAY RING COVER, REF OM271000, CONTAINS (1) TRAY RING COVER, STERILE R, Rx Only, — FDA record Z-1033-2022 | Is It on Recall"
description: "Potential breach in the sterility barrier for tray ring covers."
url: https://isitonrecall.com/recall/fda-device-z-1033-2022-tray-ring-cover-ref-om271000-contains-1-tray-ring-cover-sterile-r-rx-only/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# TRAY RING COVER, REF OM271000, CONTAINS (1) TRAY RING COVER, STERILE R, Rx Only, — FDA record Z-1033-2022

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 Apr 6, 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**: TRAY RING COVER, REF OM271000, CONTAINS (1) TRAY RING COVER, STERILE R, Rx Only,
- **Reason**: Potential breach in the sterility barrier for tray ring covers.
- **Classification**: Class II
- **Recalling firm**: Johnson & Johnson Surgical Vision Inc
- **Quantity**: N/A
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1033-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1033-2022%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 | All Lots within Expiry: GTIN:05050474520707 |

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

## Distribution

Worlwide distribution - US Nationwide distribution in the states of AL, AR, AZ, CA, FL, GA, HI, IL, IN, KS, MA, MD, MN, MO, NC, NE, NJ, NM, NV, NY, OH, OR, PA, TN, TX, WA, WI and the countries of Chile, Indonesia, India, Japan, Malaysia, Philippines, Taiwan.

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

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## Dates in the source

- **Report date**: May 11, 2022
- **Recall initiation date**: Apr 6, 2022
- **Center classification date**: May 4, 2022

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-1033-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Johnson & Johnson Surgical Vision Inc records](https://isitonrecall.com/brand/johnson-johnson-surgical-vision-inc/)
