CLASS I Device recall · Reported 26 Sep 2012 · FDA Enforcement Report

CMS-8495-R5 Custom Vein Tray containing bottle PVP Prep Solution recalled

Custom Medical Specialties is recalling CMS-8495-R5 Custom Vein Tray containing bottle PVP Prep Solution, distributed nationwide in the US. The recall was initiated on 30 Sep 2011 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codes15924-0906, 16975-0910, 17709-0912
Quantity recalled15 cases

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-2356-2012
FDA event ID
62132
Recalling firm
Custom Medical Specialties, Pine Level, NC
Classification
Class I
Status
Terminated
Recall initiated
30 Sep 2011
FDA classified
20 Sep 2012
Reported
26 Sep 2012
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Other Reasons

Timeline

30 Sep 2011Recall initiated by company
20 Sep 2012Classified by FDA+356 days
26 Sep 2012Published in enforcement report+6 days

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

Reason for recall

The firm saw on the FDA web site a recall by the manufacturer of the Povidone Iodine Prep Solution due to no microbial testing and product did not meet proper finished goods specifications.

Product as listed by the FDA

CMS-8495-R5 Custom Vein Tray containing 4 oz. bottle PVP Prep Solution Product Usage: Usage: The PVP contained in the kit is used in skin prep

Where it was distributed

US Nationwide Distribution including the states of CO, FL, KS, MA, MI, NJ and PA.

Nationwide ColoradoFloridaKansasMassachusettsMichiganNew JerseyPennsylvania

Questions about this recall

Why was it recalled?

The firm saw on the FDA web site a recall by the manufacturer of the Povidone Iodine Prep Solution due to no microbial testing and product did not meet proper finished goods specifications.

Which lots are affected?

15924-0906, 16975-0910, 17709-0912

Where was it sold?

US Nationwide Distribution including the states of CO, FL, KS, MA, MI, NJ and PA.

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

Other products in this recall event

11 other products · FDA event 62132

This product is part of a recall event; the main page for the event is CMS-8450-R1 Custom Vein Tray containing bottle PVP Prep Solution recalled.

More recalls from Custom Medical Specialties

All 21

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