June 2018 FDA Recall Kit For The Preparation Of Technetium Tc 99m Medronate by Pharmalucence, Inc.
D-1040-2018 - Lack of assurance of sterility

This Class II drug recall was voluntarily initiated by Pharmalucence, Inc. on June 6, 2018 for the product Kit For The Preparation Of Technetium Tc 99m Medronate. The FDA reported the reason for recall as lack of assurance of sterility. The product was distributed Nationwide and the recall is currently terminated.

Recall Number: D-1040-2018

Reason for Recall
Lack of assurance of sterility: Technetium TC-99M Medronate Kit has a reported breach of sterility.
Initiated
06-06-2018
Reported
08-15-2018
Quantity
95 kits

Recall Profile & Regulatory Data

Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Kit for the Preparation of Technetium Tc99m Medronate, 20mg in 10 mL vial, packaged in a) 5-count box (NDC 45567-0040-1), b) 30-count box, NDC 45567-0040-2 , Rx only, Manufactured by: Pharmalucence, Inc., Billerica, MA 01821.

Batch or Lot Expiration Information

Lot# Lot 4223