Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0921-2014 — B. Braun AccuFlo Elastomeric Infusion Pump 200ML/H 100 ML Generally used for delivery of antibiotic and local anesthesia medications.

U.S. FDA — Device Enforcement · United States · 2013-12-13 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0921-2014
Date of alert
2013-12-13
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
B. Braun Medical, Inc.
Product category
device
Product type
Devices
Reported risk: Internal testing of two lots of the AccuFlo CT-2000-100 Elastomeric Infusion Pump identified flow rates which are outside the specified infusion time and may result in overly rapid infusion of medications.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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