Data Foundry

Medical device recalls 2021

15 drops/ml — Class II medical device recall Z-2544-2021

Terminated recall by B. Braun Medical, Inc., reported 2021-10-06, distributed nationwide. Leakage of the pump set within the cassette portion of the pump sets, potential for delays in administration o

Recall numberZ-2544-2021
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmB. Braun Medical, Inc., Allentown, PA, United States
Recall initiated2021-08-10
Classified2021-09-24
Reported by FDA2021-10-06
Terminated2024-09-16
DistributedNationwide (US)
Countries outside the USCA
Quantity978,876 units
Reason classespackaging
UPC / GTIN / UDI-DI04046964293832
Lot numbers0061752459, 0061752460, 0061755100, 0061755637, 0061757837, 0061757838, 0061758588, 0061759428, 0061759475, 0061761605, 0061765911, 0061766189, 0061767026, 0061767841, 0061769047, 0061769091, 0061769931, 0061770185, 0061770486, 0061771274, 0061772190, 0061775452, 0061776078, 0061776101, 0061776773, 0061776915, 0061777160, 0061777161, 0061780362, 0061780840, 0061781779, 00VL752554

Product

15 drops/ml, Priming Volume: 27ml, Length: 129 in. Single-use for use with the Outlook Safety Infusion System and/or Horizon NXT Pump for infusion of parenteral fluid Material ID: 354212

Reason for recall

Leakage of the pump set within the cassette portion of the pump sets, potential for delays in administration of medications, under-delivery or incomplete dosing and bloodstream infections.

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-2544-2021. 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.