DOSI-FUSER 12591 5-500D1 -USA, 12591 5-600D1 -USA Provide parenteral drug infusions at a constant flow without impeding patient mobility
- Recall Initiated
- May 23, 2019
- Terminated
- June 8, 2020
- Recall Number
- Z-2360-2019
- Quantity
- 1700
Reason for Recall
The product lacks 510(k) clearance, and therefore is misbranded and must be removed from the U.S. market.
Distribution
US Distribution to states in: AZ, CA, MA, MI, PR, and FL.
Lot / Code Info
172055L, 1721 10L, 1 807881, 181 1401 Unique Device Identifier (UDI) 08436020767470, 08436020768026
Root Cause
No Marketing Application
Action Taken
The Firm, LEVENTON, S.A.U., notified customers of recall on June 4, 2019. Distributors were asked to inform customers of the recall. Customers were instructed to return all unused product to the distributor. Distributors were told to destroy all returned product and any remaining product in inventory. Distributors were also provided with recall response forms to complete and return to the recalling firm. If you have questions or concerns, please contact: Quality Director LEVENTON S.A.U. Phone: + 34 93 8176316, Fax: +34 93 8176301 email : dsalvatierra@leventon.es