Baxter FloSeal Hemostatic Matrix RECOTHROM, Product Codes: a) ADS202105, 5mL-6 PK US b) ADS202110, 10mL US
FDA Recall Z-0662-2024 · Posted 2024-01-05
Advertisement
Recalling FirmBaxter Healthcare Corporation
Recall StatusOpen, Classified
Product CodeLMF
Date Initiated2023-12-06
Reason for Recall
Cardiovascular Surgery marketing brochure (US-AS46-220001) that was distributed for the products listed below contains inaccurate content that does not align with some of the products Instructions for Use (IFU) or Prescribing Information (PI).
Firm Action
Baxter issued an IMPORTANT PRODUCT INFORMATION to its consignees on 12/06/2023 via USPS first class mail. The notice explained the issue, potential hazard involved, and requested the following:
Actions to be Taken by Customers:
1. Healthcare providers may continue to safely use the products listed above while
following the associated Instructions for Use.
2. Cease any further distribution of the Cardiovascular Surgery marketing brochure
for the products listed above. All copies of this marketing brochure should be
promptly discarded. The brochure reference number, US-AS46-220001, can be
found at the bottom of the last page of the brochure.
3. If you received this communication directly from Baxter, please
acknowledge receipt by responding on our customer portal at
https://BaxterFieldActionCustomerPortal.onprocess.com, even if you do
not have any inventory. Log in to the portal using the account number listed on
the enclosed reply form instruction sheet. Acknowledging receipt of this
notification will prevent you from receiving repeat notices. If you do not complete
the acknowledgement, you will receive a phone call from OnProcess Technology
on behalf of Baxter to confirm your receipt of this notification.
4. If you purchased this product from a distributor, please note that responding on
the Baxter customer portal is not applicable. If a response is requested by your
distributor or wholesaler, please respond to the supplier according to their
instructions.
5. If you distributed a copy of this brochure to other facilities or departments within
your institution, please forward a copy of this communication to them.
6. If you are a dealer, wholesaler, distributor/reseller, or original equipment
manufacturer (OEM) that distributed any copies of the brochure to other facilities,
please distribute this notification to customers and check the associated box on
the customer portal.
For general questions, contact Baxter Healthcare Center for Service at 888-229-0001,
betwe
Root Cause
Under Investigation by firm
Distribution Pattern
US Nationwide distribution.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
Advertisement