LAPAROSCOPY GYN PACK — Class I medical device recall Z-2335-2014
Terminated recall by Customed, Inc, reported 2014-09-10, distributed nationwide. Customed has determined that there is the possibility that packaging integrity may be compromised on different
| Recall number | Z-2335-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Customed, Inc, Fajardo, PR, United States |
| Recall initiated | 2014-05-20 |
| Classified | 2014-08-29 |
| Reported by FDA | 2014-09-10 |
| Terminated | 2017-08-14 |
| Distributed | Nationwide (US) |
| Countries outside the US | CR, DO, MX, TT |
| Reason classes | sterility, packaging |
| Lot numbers | 110092266, 110102447, 110112666, 110123109, 111010142, 111020291, 111030694, 111040908, 111061557, 111071939, 111082104, 111092395, 111102768, 111113129, 111123270, 112010189, 112020490, 112030886, 112051997, 112062497, 112072807, 112083435, 112093728, 112124593, 112125104, 113078336, 113088877, 113099445, 113109859, 131110267, 131210832, 140111091, 140312177, 140412696 |
Product
LAPAROSCOPY GYN PACK - - (1) BLADE SURGICAL #11 STAINLESS STEEL (4) DRAPE UTILITY WITH TAPE LIF (2) ABSORBENT TOWEL 15" X 20" LIF (1) GOWN IMPERVIOUS REINFORCED LARGE SMS (1) TOWEL CLOTH HUCK BLUE (1) BLADE SURGICAL #15 CARBON STEEL (2) UTILITY BOWL 16oz (1) UTILITY BOWL 32oz (2) LEGGINS WITH 7" CUFF 30" X 42" LIF (1) EMESIS BASIN 10in 700cc (1) DRAPE VIDEO CAMERA 13cm X 244cm LIF (1) MAYO STAND COVER REINFORCED LIF (10) GAUZE SPONGES 4" X 4" 16PLY XRD LIF (2) TUBE SUCTION CONNECT 114" X 12' LIF (1) TABLE COVER REINFORCED 44" X 78" UF (1) DRAPE LAP. PERINEAL 102" X 97" WITH POUCH (1) GOWN SURGICAL REINFORCED LARGE TOWEL/WRAP EO sterilized surgical convenient packs packaged into polyester/polyethylene breather bag with Tyvek double vents.
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2335-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.