---
title: "NATURALYTE Liquid Acid 2.0K 2.5Ca- indicated for use in patients undergoing e... — FDA record Z-1370-2022 | Is It on Recall"
description: "Alternate Bottle Caps labeled with \"Sealed for your Protection\" on the foil not qualified for use"
url: https://isitonrecall.com/recall/fda-device-z-1370-2022-naturalyte-liquid-acid-2-0k-2-5ca-indicated-for-use-in-patients-undergoing-extracorporeal-bicarbonat/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# NATURALYTE Liquid Acid 2.0K 2.5Ca- indicated for use in patients undergoing extracorporeal bicarbonate hemodialysis f... — FDA record Z-1370-2022

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 May 31, 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**: NATURALYTE Liquid Acid 2.0K 2.5Ca- indicated for use in patients undergoing extracorporeal bicarbonate hemodialysis for acute and chronic renal failure Part Number: 08-2251-0
- **Reason**: Alternate Bottle Caps labeled with "Sealed for your Protection" on the foil not qualified for use
- **Classification**: Class II
- **Recalling firm**: Fresenius Medical Care Holdings, Inc.
- **Quantity**: 656 cases
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1370-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1370-2022%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 | UDI-DI: (01) 000840861101696 (17) 240331 (10) 22CTAC106 Lot Number: 22CTAC106 Exp Date: 2024-03-31 |

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

## Distribution

Natiowide

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Jul 20, 2022
- **Recall initiation date**: May 31, 2022
- **Center classification date**: Jul 12, 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-1370-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Fresenius Medical Care Holdings, Inc. records](https://isitonrecall.com/brand/fresenius-medical-care-holdings-inc/)