Data Foundry

Drug recalls 2021

DELFLEX Peritoneal Dialysis Solution with 2 — Class III drug recall D-0605-2021

Terminated recall by Fresenius Medical Care Holdings, Inc., reported 2021-06-16, distributed nationwide. Temperature Abuse: Product exposed to temperature outside specified limits.

Recall numberD-0605-2021
Product typeDrug
ClassificationClass III
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmFresenius Medical Care Holdings, Inc., Waltham, MA, United States
Recall initiated2021-04-28
Classified2021-06-09
Reported by FDA2021-06-16
Terminated2021-09-17
DistributedNationwide (US)
Quantity672 cases
Reason classestemperature control
NDC49230-0206, 49230-0206-30, 49230-0206-32, 49230-0206-50, 49230-0206-52, 49230-0206-62, 49230-0209, 49230-0209-23, 49230-0209-30, 49230-0209-32, 49230-0209-50, 49230-0209-52, 49230-0209-62, 49230-0212, 49230-0212-30, 49230-0212-32, 49230-0212-50, 49230-0212-52, 49230-0212-62
Expiration dates2022-06-20, 2022-07-20, 2022-08-20

Product

DELFLEX Peritoneal Dialysis Solution with 2.5 % Dextrose, Low Magnesium, Low Calcium, packaged in a) 3000 mL 2 packs (NDC 49230-0209-23), b) 3000 mL (NDC 49230-209-30) and c) 5000 mL (NDC 49230-209-50) Rx only, Fresenius Medical Care NA Waltham, MA 02451

Reason for recall

Temperature Abuse: Product exposed to temperature outside specified limits.

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/D-0605-2021. 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.