Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
Z-1638-2018Class II

Maximum Barrier Tray

Vygon U.S.A. / initiated 2018-02-28 / Terminated / root cause: sterility

Vygon U.S.A. began a recall of Maximum Barrier Tray, Product Code: MCITX-1 Convenience kit for the insertion of PICCs into the vascular system on . FDA classified it as Class II and gives the reason as "Potential friction holes may affect the sterility of the product". As of , the recall status on record is Terminated, and MDM tags the root cause as sterility.

Recall record

Recall number
Z-1638-2018
Classification
Class II
Status
Terminated
Initiated
Posted
Terminated
Recalling firm
Vygon U.S.A.
Product
Maximum Barrier Tray, Product Code: MCITX-1 Convenience kit for the insertion of PICCs into the vascular system.
Product code
OWL Peripheral Catheter Insertion Kit
Reason for recall
Potential friction holes may affect the sterility of the product.
Root cause tag
sterility
FDA root cause
Under Investigation by firm
Action
The firm, Vygon USA, mailed an "URGENT MEDICAL DEVICE RECALL" letter dated 2/28/2018 to affected customers. The letter described the product, problem and actions to be taken. The Customers are instructed to: 1) Check your stock for the products included within the scope of the recall. Immediately cease use and distribution, and quarantine all affected product immediately; 2) Count and document your affected inventory on the Recall Acknowledgement and Inventory Return Form; 3) complete and return form via Fax to 215-672-6740 or email to: [email protected] including customer contact information; 4) Vygon customer service will contact the customer and issue a Return Merchandise Authorization number; 5) Return the product as well as the original signed Recall Acknowledgement and Inventory Return Form using the instructions from Customer Service involving product pick-up. Distributors are instructed to: communicate the recall to customers who received the affected product by providing them a copy of the notification. Also, provide a copy of the Recall Acknowledgement and Inventory Return Form to customers. If you have questions or concerns please contact your local sales representative or Vygon's Customer Service Department at 1-800-473-5414, or by e-mail at [email protected].
Quantity in commerce
16,520 total products
Distribution
Nationwide Distribution to states of: AZ, UT, WI, NJ, CT, TX, PA, VA, MN, MA, MO, FL, and CA.
Product codes and lots
Lot Numbers: 16I025D, 16L026D, 17C014D UDI: 08498840009604

Enforcement reports

One row per recalled product line
FDA enforcement reports joined to recall event Z-1638-2018
Recall numberClassStatusVoluntary or mandatedReport dateClassified
Z-1633-2018Class IITerminatedVoluntary: Firm initiated
Z-1634-2018Class IITerminatedVoluntary: Firm initiated
Z-1635-2018Class IITerminatedVoluntary: Firm initiated
Z-1636-2018Class IITerminatedVoluntary: Firm initiated
Z-1637-2018Class IITerminatedVoluntary: Firm initiated
Z-1638-2018Class IITerminatedVoluntary: Firm initiated
Z-1639-2018Class IITerminatedVoluntary: Firm initiated
Z-1640-2018Class IITerminatedVoluntary: Firm initiated