EXCOR Pediatric Ventricular Assist Device (VAD) System Blood Pump PU Valves: 10 ml, REF: P10P-001; 30 ml, REF: P30P-001x01
FDA Recall Z-2320-2026 · Posted 2026-06-05
Recalling FirmBERLIN HEART GMBH
Recall StatusOpen, Classified
Product CodeDSQ
Date Initiated2026-04-24
Product Quantity3
Reason for Recall
Blood pump inner package expiration date does not match the outer-correct expiration date, which may lead to delays in surgical procedures.
Firm Action
On 4/24/2026, recall notices were emailed to customers who were asked to do the following:
1) Segregate and discontinue use of any affected unused product.
2). Notify all appropriate personnel within your organization who need to be aware of this recall.
3) If any affected devices have been transferred to another facility or customer, promptly forward this notification to those accounts.
4) Firm will provide replacement products for the affected mislabeled devices and
will issue a return shipping label so affected unused products may be returned through
the Return Goods Authorization (RGA) process.
5) Complete, sign, and return the attached Acknowledgement Form by email to
[email protected]
If you have questions, contact the firm at [email protected] or 888-826-9466
Root Cause
Error in labeling
Distribution Pattern
US Nationwide distribution in the states of MA, SC.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.