FDAFDA · Food and drugs·Recall number Z-2413-2014
LAPAROSCOPY PREMIUM PACK - (1) TABLE COVER REINFORCED 50" x 90" UF (4) TOWEL ABSORBENT 15" x 20" UF (10) GAUZE SPONGE 4" X 4" 16PLY XRD UF (1) DRAPE LASER CAMERA W/EL UF (1) TROCAR ENDO.XCEL DILATING TIP (KSLT) (1) APPLIER CLIP 5MM (3) GOWN XLGE SMS IMPERV. REINFORCED (1) BLADE SURGICAL #11 S/STEEL (1) NEEDLE PNEUMO INSUFLAT. 150MM UL UF (1) MAYO STAND COVER REINFORCED UF (1) DRAPE LAPAROSCOPY ABDOM. W/POUCH (4) DRAPE UTILITY WITH TAPE UF (1) TUBING INSUFFLATION SET W/0 RING ADAPTOR U/F (1) TROCAR DILATING XCEL 5MM x 100 (D5LT) (1) TROCAR ENDO.XCEL DILATING TIP 11MM (1) SUTURE BAG FLORAL UF (1) CLOSURE SKIN W' X 4" STERI STRIP LF EO sterilized surgical convenient packs packaged into polyester/polyethylene breather bag with Tyvek double vents.
Published September 10, 2014 · Recall initiated: May 20, 2014
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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 to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Customed, Inc
- Distributor
- 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.
- Lot
- Product code 900-1803, 7 lots: 112114857 112125169 113026230 113036759 140312276 140412556 140513115
- Risk classification
- Class I
- Area (FDA)
- device
- Country
- United States
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