Baxter Healthcare Corp. Rt. Baxter Sabraset 6060 Administration Set with Pre-attached 250 mL Bag and Cassette, product code 560500-250; Manufactured for Baxter Healthcare Corporation, Deerfield, IL 60015 U.S.A., Made in Mexico Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Baxter Sabraset 6060 Administration Set with Pre-attached 250 mL Bag and Cassette, product code 560500-250; Manufactured for Baxter Healthcare Corporation, Deerfield, IL 60015 U.S.A., Made in Mexico
Brand
Baxter Healthcare Corp. Rt.
Lot Codes / Batch Numbers
product code 560500-250, lots 417521, 418481, 418744
Products Sold
product code 560500-250, lots 417521, 418481, 418744
Baxter Healthcare Corp. Rt. is recalling Baxter Sabraset 6060 Administration Set with Pre-attached 250 mL Bag and Cassette, product code 5605 due to The inlet and outlet lines of the administration set may be reversed, which would result in reverse flow.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The inlet and outlet lines of the administration set may be reversed, which would result in reverse flow.
Recommended Action
Per FDA guidance
Baxter sent Urgent Device Correction letters dated 5/4/05 to their customers, to the attention of the Director of Nursing, via first class mail on the same date. The accounts were informed of the one complaint of reverse assembly of the administration set, and were provided with diagrams showing the configuration of a correct assembly and an incorrect assembly of the sets. The accounts were instructed to inspect the sets carefully before use to assure correct assembly. The accounts were requested to destroy any misassembled sets found and complete the certificate of destruction enclosed with the letter, faxing it back to Baxter at 847-270-5457 to receive credit for the destroyed sets.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026