Archived Content

The content on this page is provided for reference purposes only. This content has not been altered or updated since it was archived.

Medical Devices

Lee Medical International Inc., Custom Dialysis Trays/Kits

Recall Class: Class I

Date Recall Initiated: March 22, 2011

Products: Custom Dialysis Trays/Kits (For product names, lot/serial numbers, expiration dates, and BIN numbers, please see table below).

These products were manufactured from January 13, 2011 through March 21, 2011 and distributed from February 9, 2011 through March 21, 2011.

See related recall under Additional Links below.

Use: The custom dialysis trays/kits are designed to include all the components (gloves, bandages, fistula needles, antibacterial pads [Povidone Iodine (PVP) Prep Pads], and specific bloodlines) used in preparing hemodialysis vascular access sites for patients undergoing dialysis procedures.

Recalling Firm:
Lee Medical International, Inc.
612 Distributors Row
Harahan, Louisiana 70123-3206

Reason for Recall: These custom dialysis trays/kits contain PVP Prep Pads that were recalled by H & P Industries. The pads may not be sterile. Patients receiving hemodialysis who use the pads may be at potential risk for serious or life threatening infection.

Public Contact: Customers may contact the company at 1-800-433-8950.

FDA District: New Orleans

FDA Comments:

Summary of Recall: On March 22, 2011, the company notified their customers (hospitals and clinics) by email and by telephone.

Product Names, Lot Numbers, Expiration Dates, BIN Numbers
  • KIDNEYCARE, 125/CS, LOT #A1160, EXP 7-12, BIN 35A
  • MESCALERO-HEMO, 200/CS, LOT #B1113, EXP 8-12
  • DAV-MT-POCONO-H, 200/CS, LOT #B1123, EXP 8-12, BIN 45B
  • ADV-CATH-ISL44, 100/CS, LOT #B1127 EXP 8-12, BIN 34B
  • ADV-HEMO-15G, 100/CS, LOT #B1128, EXP 8-12, BIN 34A
  • NORTHHUDSON-C, 100/CS, LOT #B1134, EXP 8-12, BIN 42B
  • NORTHHUDSON-H, 75/CS, LOT #B1135, EXP 8012, BIN 42B
  • JOHNHAYES-HEMO, SMALL GLOVES, 100/CS, LOT #B1143, B1144, and B1145. EXP 8-12
  • SNCH-CATH, 50/CS, LOT #B1152, EXP 8-12, BIN 43A
  • COMMUNITY-HEMO, 125/CS, LOT #B1156, EXP 8-12
  • FLAMS-HEMO, 125/CS. LOT #B1162, EXP 8-12, BIN 38B
  • KINDEYSPA-HEMO, 125/CS, LOT #B1161, EXP 8-12, BIN 35B
  • DAV-POCONO-H, 500/CS, LOT #C1107, EXP 9-12
  • DAV-POCONO-CATH, 75/CS, LOT #C1108, EXP 9-12, BIN 43B
  • DAV-MT-POCONO-H, 200/CS, LOT #C1109, EXP 9-12
  • MESCALERO-HEMO, 200/CS, LOT #C1110, EXP 9-12
  • KIDNEYTRMT-HEMO, 125/CS, LOT #C1112 and C1123, EXP 9-12, BIN 45A
  • DAV-POCONO-H, 500/CS, LOT #C1126, EXP 9-12
  • METHODIST-HEMO, 150/CS, LOT #C1139, EXP 9-12
  • KINGMAN-HEMO, 150/CS, LOT #C1141, EXP 9-12
  • DAV-PALMERTON-H, 200/CS, LOT #C1145, EXP 9-12, BIN 43B
  • EMANUEL-CATH, 100/CS, LOT #C1146, EXP 9-12, BIN 34B

Class 1 recalls are the most serious type of recall and involve situations in which there is a reasonable probability that use of these products will cause serious adverse health consequences or death.

Health care professionals and consumers may report adverse reactions or quality problems they experienced using these products to MedWatch: The FDA Safety Information and Adverse Event Reporting Program either online, by regular mail or by FAX.

Additional Links:


Page Last Updated: 02/06/2014
Note: If you need help accessing information in different file formats, see Instructions for Downloading Viewers and Players.