Clark Research and Development Inc Number Clark Biocompatible Hemoperfusion Cartridge, Sorbent: Heparinized polymer over acitivated carbon, 50mL, Clark Research and Development, Inc. Folsom, LA 70437 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Clark Biocompatible Hemoperfusion Cartridge, Sorbent: Heparinized polymer over acitivated carbon, 50mL, Clark Research and Development, Inc. Folsom, LA 70437
Brand
Clark Research and Development Inc Number
Lot Codes / Batch Numbers
Lot numbers 564 though 577
Products Sold
Lot numbers 564 though 577
Clark Research and Development Inc Number is recalling Clark Biocompatible Hemoperfusion Cartridge, Sorbent: Heparinized polymer over acitivated carbon, 5 due to Lack of sterility assurance based on lack of sterility validation for labeled sterilization directions. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Lack of sterility assurance based on lack of sterility validation for labeled sterilization directions
Recommended Action
Per FDA guidance
The firm notified its consignees of the problem and the recall via letter (priority mail with delivery confirmation)dated 01/19/2007 beginning on 01/19/2007. This letter requested that the consignee cease the use of this product and contact the recalling firm for return instructions. Follow-up with non-reponders will be made by facsimile.
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