---
title: "BAUSCH + LOMB CATARACT PACK, REF VAL009CTSGA. Convenience kit used in surgica... — FDA record Z-0158-2023 | Is It on Recall"
description: "Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal."
url: https://isitonrecall.com/recall/fda-device-z-0158-2023-bausch-lomb-cataract-pack-ref-val009ctsga-convenience-kit-used-in-surgical-procedures/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# BAUSCH + LOMB CATARACT PACK, REF VAL009CTSGA. Convenience kit used in surgical procedures. — FDA record Z-0158-2023

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 Sep 30, 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**: BAUSCH + LOMB CATARACT PACK, REF VAL009CTSGA. Convenience kit used in surgical procedures.
- **Reason**: Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal.
- **Classification**: Class II
- **Recalling firm**: MEDLINE INDUSTRIES, LP - Northfield
- **Quantity**: 300 kits
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0158-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0158-2023%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 (01) 40193489577540, Lot Number 22DBN862 |

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

## Distribution

US Nationwide distribution in the states of CA, MN, NC, NY, OK, PA, TN, TX.

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

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- [Oregon](https://isitonrecall.com/state/oregon/)
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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Nov 9, 2022
- **Recall initiation date**: Sep 30, 2022
- **Center classification date**: Nov 1, 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-0158-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [MEDLINE INDUSTRIES, LP - Northfield records](https://isitonrecall.com/brand/medline-industries-lp-northfield/)
