FDAClass ISeptember 10, 2014

Perl GYN Pack recall: Sterility Concern

PERl GYN PACK (1) TABLE COVER 44" x 90" (2) LEGGINS W/7" CUFF 30" x 42" (1) ABDOMINAL DRAPE WITH TAPE LIF (2) TOWELS ABSORBENT 15" X 20" (10) GAUZE…

Why was Perl GYN Pack recalled?

Customed has determined that there is the possibility that packaging integrity may be compromised on different catalog numbers (multiple lots). This could result in an injury to the patient due to product contamination or loss of sterility condition.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Product code 900-997, 54 lots: 109010132 109020292 109061223 109061459 109081892 109092100 109102355 109112608 109122830 110010122 110030692 110030798 110061476 110071720 110081986 110092293 110092410 110112818 111010176 111020308 111030676 111041119 111051306 111061572 111071842 111082121 111082231 111092411 111102790 111113148 111123310 112020497 112030758 112041366 112052028 112072881 112083445 112093959 112104309 112125125 113015522 113025975 113026120 113036394 113057518 113078481 113088901 113099461 113109885 140111263 140211865 140312193 140412708 140513386

Product
PERl GYN PACK (1) TABLE COVER 44" x 90" (2) LEGGINS W/7" CUFF 30" x 42" (1) ABDOMINAL DRAPE WITH TAPE LIF (2) TOWELS ABSORBENT 15" X 20" (10) GAUZE…
Recalling firm
Customed, Inc
Quantity
54 lots; 2965 units (multiple units per lot)
Distribution
Worldwide Distribution - US (nationwide) in the state of Florida including Puerto Rico (USA); & USVI (St John) and the countries of Tortola, Trinidad, Dominican Republic, Costa Rica and Mexico.
Recall date
September 10, 2014
Classification
Class I
Status
Terminated
Agency
FDA (device)
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