CLASS I Device recall · Reported 10 Sep 2014 · FDA Enforcement Report

Strabismus & Plastic Pack - Table Cover Reinforced 44" X recalled

Customed is recalling Strabismus & Plastic Pack - Table Cover Reinforced 44" X 78" Uf Gown Standard Large Sms, distributed nationwide in the US. The recall was initiated on 20 May 2014 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesProduct code 900-946, 46 lots: 109010131 109020438 109030630 109030725 109061221 109061458 109081891 109102354 109112606 109122828 110010121 110020416 110030690 110041052 110071718 110092291 110092375 110112686 110122949 111010174 111020307 111040981 111051220 111061571 111071946 111082118 111092409 111102788 112010212 112020507 112030756 112041364 112052026 112072879 112083443 112093956 112114687 112125122 113025973 113036807 113057516 113089090 113109650 113109883 140111260 140111318

Quantity recalled46 lots; 1240 units (multiple units per lot)manufactured

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-2362-2014
FDA event ID: 68536
Recalling firm: Customed, Fajardo, PR
Classification: Class I
Status: Terminated
Recall initiated: 20 May 2014
FDA classified: 29 Aug 2014
Reported: 10 Sep 2014
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Foreign Material
Device type: Surgical Instruments

Timeline

20 May 2014	Recall initiated by company
29 Aug 2014	Classified by FDA	+101 days
10 Sep 2014	Published in enforcement report	+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

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.

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

STRABISMUS & PLASTIC PACK - (1) TABLE COVER REINFORCED 44" X 78" UF (2) GOWN STANDARD LARGE SMS (3) TOWELS ABSORBENT 15" X 20" UF (1) MAYO STAND COVER REINFORCED UF (1) DRAPE SHEET 41" X 58" SMS (4) DRAPE UTILITY WITH TAPE L/F EO sterilized surgical convenient packs packaged into polyester/polyethylene breather bag with Tyvek double vents.

Where it was distributed

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.

Nationwide Florida Puerto Rico

Questions about this recall

Is Strabismus & Plastic Pack - Table Cover Reinforced 44" X 78" Uf Gown Standard Large Sms recalled?

Yes. Customed recalled Strabismus & Plastic Pack - Table Cover Reinforced 44" X 78" Uf Gown Standard Large Sms on 20 May 2014. The recall is Class I and its status is Terminated. Recall number Z-2362-2014.

Why was it recalled?

Which lots are affected?

Product code 900-946, 46 lots: 109010131 109020438 109030630 109030725 109061221 109061458 109081891 109102354 109112606 109122828 110010121 110020416 110030690 110041052 110071718 110092291 110092375 110112686 110122949 111010174 111020307 111040981 111051220 111061571 111071946 111082118 111092409 111102788 112010212 112020507 112030756 112041364 112052026 112072879 112083443 112093956 112114687 112125122 113025973 113036807 113057516 113089090 113109650 113109883 140111260 140111318

Where was it sold?

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.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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