Vygon Corporation: Medical Device Recall in 2012 - (Recall #: Z-1807-2012)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

Churchill Medical Systems, Inc. DRESSING CHANGE KIT Prefilled syringes included in the kit are used to maintain the patency of indwelling catheter lumens

Product Classification:

Class II

Date Initiated: May 11, 2012

Date Posted: June 20, 2012

Recall Number: Z-1807-2012

Event ID: 61945

Reason for Recall:

Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush Heparin Lock Flush Syringes therefore Vygon has subsequently initiated a recall on Vygon branded Heparin Lock Flush Syringes and kits containing the syringes.

Status: Terminated

Product Quantity:

Code Information:

Product Code AMS-7091CP - lot 11C119.

Distribution Pattern:

Nationwide Distribution including AZ, CA, DE, FL, IL, IN, IA, KS, KY, MD, MA, MI, MN, MO, NJ, NY, OH, PA, UT, VA, WA, WV, and WI.

Voluntary or Mandated:

Voluntary: Firm initiated