CLASS II Device recall · Reported 12 Apr 2017 · FDA Enforcement Report

Ophthalmic Dressing Tray The Covidien Curity Oval Eye Pads recalled

Centurion Medical Products is recalling Ophthalmic Dressing Tray The Covidien Curity Oval Eye Pads are individually packaged and, distributed in 9 states. The recall was initiated on 9 Mar 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesCenturion component code 2841, Affected product was placed into Centurion Convenience Kits between July 2013 and January 2017. Batch Numbers & Exp. dates: 2016081750 4/30/19 2016080450 12/31/18 2016060250 10/31/18 2015091050 4/30/18 2015090350 4/30/18 2015083150 4/30/18 2015012750 10/31/17 2015012250 10/31/17 2014061850 4/30/17

Quantity recalled210 kits

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-1731-2017
FDA event ID: 76730
Recalling firm: Centurion Medical Products, Williamston, MI
Classification: Class II
Status: Terminated
Recall initiated: 9 Mar 2017
FDA classified: 5 Apr 2017
Reported: 12 Apr 2017
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Sterility
Device type: Test Kits & Diagnostics

Timeline

9 Mar 2017	Recall initiated by company
5 Apr 2017	Classified by FDA	+27 days
12 Apr 2017	Published in enforcement report	+7 days

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

Reason for recall

Centurion Medical Products is recalling Convenience Kits that contain Covidien Curity Oval Eye Pads due to supplier's recall because of potential breach in sterile packaging.

A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.

Product as listed by the FDA

OPHTHALMIC DRESSING TRAY The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer; they are then placed into non-sterile Centurion Convenience Kits along with other components.

Where it was distributed

US Distribution: NY, NC, PA, CA, OH, WA, VA, NJ, IL

California Illinois North Carolina New Jersey New York Ohio Pennsylvania Virginia Washington

Questions about this recall

Is Ophthalmic Dressing Tray The Covidien Curity Oval Eye Pads are individually packaged and recalled?

Yes. Centurion Medical Products recalled Ophthalmic Dressing Tray The Covidien Curity Oval Eye Pads are individually packaged and on 9 Mar 2017. The recall is Class II and its status is Terminated. Recall number Z-1731-2017.

Why was it recalled?

Centurion Medical Products is recalling Convenience Kits that contain Covidien Curity Oval Eye Pads due to supplier's recall because of potential breach in sterile packaging.

Which lots are affected?

Centurion component code 2841, Affected product was placed into Centurion Convenience Kits between July 2013 and January 2017. Batch Numbers & Exp. dates: 2016081750 4/30/19 2016080450 12/31/18 2016060250 10/31/18 2015091050 4/30/18 2015090350 4/30/18 2015083150 4/30/18 2015012750 10/31/17 2015012250 10/31/17 2014061850 4/30/17

Where was it sold?

US Distribution: NY, NC, PA, CA, OH, WA, VA, NJ, IL

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

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.

More recalls from Centurion Medical Products

All 152

Reported	Class	Recall	Company	Reason	Where
15 Jul 2020Device	CLASS II	Centurion Difficult IV KIT containing BD's Vacutainer recalled	Centurion Medical Products	Foreign Material	Nationwide
12 Feb 2020Device	CLASS II	Centurion-Lvad Kits DM1005 Daily Lvad Maintenance Kit recalled	Centurion Medical Products	Lead & Heavy Metals	Nationwide
12 Feb 2020Device	CLASS II	Centurion- Pelvic Exam Kits DYNDE1037 Pelvic Exam recalled	Centurion Medical Products	Sterility	Nationwide
12 Feb 2020Device	CLASS II	Centurion- SPEC0002B Arthrogram Tray SPEC0002B Arthrogram recalled	Centurion Medical Products	Sterility	Nationwide
12 Feb 2020Device	CLASS II	Centurion-Irrigation Kit IG25STSS Irrigation Gun &Valve Set recalled	Centurion Medical Products	Sterility	Nationwide

Other Test Kits & Diagnostics recalls

All 2,656

Reported	Class	Recall	Company	Reason	Where
9 Sep 2026Device	CLASS II	STA Staclot Protein S recalled by Diagnostica Stago	Diagnostica Stago	Potency & Assay	Nationwide
26 Aug 2026Device	CLASS II	DxC 500i Clinical Analyzer Modules using recalled by Beckman Coulter	Beckman Coulter	Packaging Defects	Nationwide
26 Aug 2026Device	CLASS II	DxC 500 AU Clinical Analyzer Modules using recalled by Beckman Coulter	Beckman Coulter	Packaging Defects	Nationwide
26 Aug 2026Device	CLASS II	Syva EMIT 2000 Quinidine Assay recalled	Siemens Healthcare Diagnostics	Lead & Heavy Metals	Nationwide
26 Aug 2026Device	CLASS II	Beckman Coulter, Emit 2000 Quinidine Assay recalled	Siemens Healthcare Diagnostics	Lead & Heavy Metals	Nationwide