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U.S. Department of Health and Human Services

Class 2 Device Recall Medline Total Knee CDS

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 Class 2 Device Recall Medline Total Knee CDSsee related information
Date Initiated by FirmSeptember 20, 2012
Date PostedDecember 17, 2012
Recall Status1 Terminated 3 on December 17, 2012
Recall NumberZ-0532-2013
Recall Event ID 63520
Product Classification General surgery tray (kit) - Product Code LRO
ProductMedline Total Knee CDS; a single patient prescription procedure pack and disposables, including a back table cover; Product Usage: This Complete Delivery Systems (CDS) custom pack includes components necessary for a total knee replacement surgical procedure.
Code Information Reorder #CDS983828, lot numbers 12HD0901 and 12IB1848, expiration date 09/30/2013
Recalling Firm/
Manufacturer		 Medline Industries Inc
1 Medline Pl
Mundelein IL 60060
For Additional Information Contact
847-949-3051
Manufacturer Reason
for Recall		The Back Table Cover component in the custom pack was placed in the non-sterile portion of the pack when it should have been in the sterile portion.
FDA Determined
Cause 2		Packaging
ActionMedline Industries Inc notified the sole direct account on September 20, 2012 via telephone that the affected custom pack were recalled. Instruction was provided to the staff at the facility not to use the pack until it had been reworked with a sterile back table cover.
Quantity in Commerce18 packs
DistributionUS (nationwide) in the state of West Virginia
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
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