---
title: "FUSION Dual Pump Packs, REF: OPO73 — FDA record Z-1006-2023 | Is It on Recall"
description: "Weld protrusion/physical gap between the housing and phaco pack cover, may exceed design specification, which could lead to priming cycle failure and/or subopti"
url: https://isitonrecall.com/recall/fda-device-z-1006-2023-fusion-dual-pump-packs-ref-opo73/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# FUSION Dual Pump Packs, REF: OPO73 — FDA record Z-1006-2023

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 Dec 7, 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**: FUSION Dual Pump Packs, REF: OPO73
- **Reason**: Weld protrusion/physical gap between the housing and phaco pack cover, may exceed design specification, which could lead to priming cycle failure and/or suboptimal vacuum delivered to the phacoemulsification and irrigation/aspiration handpieces during surgery, which could result in surgical delay and/or longer surgical time, which could result in transient corneal edema.
- **Classification**: Class II
- **Recalling firm**: Johnson & Johnson Surgical Vision, Inc.
- **Quantity**: 7644
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1006-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1006-2023%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 | UDI-DI/Lots: 15050474602080/60373238, 60394037, 60308197 |

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

## Distribution

US: FL, MS, NY, TN, TX, IL, MN, OH. OUS: Belgium, China, Estonia, France, Germany, Indonesia, Italy, Japan, Malaysia, Netherlands, Portugal, Sri Lanka, Switzerland, Thailand, United Kingdom

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

- [Florida](https://isitonrecall.com/state/florida/)
- [Illinois](https://isitonrecall.com/state/illinois/)
- [Minnesota](https://isitonrecall.com/state/minnesota/)
- [Mississippi](https://isitonrecall.com/state/mississippi/)
- [New York](https://isitonrecall.com/state/new-york/)
- [Ohio](https://isitonrecall.com/state/ohio/)
- [Tennessee](https://isitonrecall.com/state/tennessee/)
- [Texas](https://isitonrecall.com/state/texas/)

## Dates in the source

- **Report date**: Feb 1, 2023
- **Recall initiation date**: Dec 7, 2022
- **Center classification date**: Jan 20, 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-1006-2023%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/)