NATURALYTE Liquid Acid 2 — Class II medical device recall Z-1370-2022
Ongoing recall by Fresenius Medical Care Holdings, Inc., reported 2022-07-20. Alternate Bottle Caps labeled with "Sealed for your Protection" on the foil not qualified for use
| Recall number | Z-1370-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Fresenius Medical Care Holdings, Inc., Waltham, MA, United States |
| Recall initiated | 2022-05-31 |
| Classified | 2022-07-12 |
| Reported by FDA | 2022-07-20 |
| Quantity | 656 cases |
| Reason classes | labeling |
| Lot numbers | 22CTAC106 |
| Model numbers | 08-2251-0 |
| Expiration dates | 2024-03-31 |
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 for recall
Alternate Bottle Caps labeled with "Sealed for your Protection" on the foil not qualified for use
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1370-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.