CLASS II Device recall · Reported 2 May 2018 · FDA Enforcement Report

EEA" Hemorrhoid and Prolapse Stapler Set recalled by Covidien

Covidien is recalling EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology, Product Number, distributed nationwide in the US. The recall was initiated on 9 Apr 2018 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLots: N7J1145MX, N7L0380MX, N7L0762MX, N7L1077MX, N7M0733MX,N7K0092MX, N7L0457MX, N7L0868MX, N7M0144MX, N7M0835MX, N7K0692MX, N7L0594MX, N7L0940MX, N7M0185MX N8A0144MX, N7K0693MX, N7L0676MX, N7L1076MX, N7M0732MX, N8A0166MX
Quantity recalled5547

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-1527-2018
FDA event ID
79905
Recalling firm
Covidien, North Haven, CT
Classification
Class II
Status
Terminated
Recall initiated
9 Apr 2018
FDA classified
26 Apr 2018
Reported
2 May 2018
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Packaging Defects

Timeline

9 Apr 2018Recall initiated by company
26 Apr 2018Classified by FDA+17 days
2 May 2018Published 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

There is a potential for improper welding of the yellow staple guide to the instrument. Use of a device with an improperly welded staple guide may result in improper staple formation potentially leading to bleeding or anastomotic leak.

Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.

Product as listed by the FDA

EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 3.5MM, Product Number HEM3335, GTIN Number 1 - 10884521047518, GTIN Number 2 - 20884521047515 Product Usage: The EEA Hemorrhoid and prolapse stapler set with DST Series Technology (instrument) is designed for use as a stapler instrument for control of rectal prolapse and hemorrhoid disease. The instrument places a circular, double-staggered row of titanium DST staples and removes a circular tissue specimen. The instrument is offered in a 33mm diameter size with either 3.5mm or 4.8mm staples. The accompanying accessories comprised of an access port, anoscope, and dilator. The access port aids the insertion and removal of the anoscope and the stapler device by dilating the anal sphincter throughout the procedure. The anoscope is designed to facilitate pursestring suture application above the dentate line. It is designed with a guide and markings to assist in creating a circumferential pursestring suture at a consistent placement within the rectum. The dilator is designed to aid the initial insertion of the anoscope and port by retracting the rectal tissue. Both the anoscope and port are transparent to facilitate visualization of the anal canal. The EEA Hemorrhoid and prolapse stapler set with DST Series Technology has application throughout the anal canal to perform surgical treatment of hemorrhoidal disease. The EEA Hemorrhoid and prolapse stapler also has application in the distal alimentary tract for the creation of end-to-end and end-to-side anastomoses.

Where it was distributed

Worldwide Distribution - US Nationwide in the US states of : AL, CA, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, NE, NJ, NY, OH, OR, SC, TN, TX, UT, and VA. The devices were distributed to the following foreign countries: UAE, Australia, Austria, Belgium, Bulgaria, Canada, Czech Republic, Denmark, Estonia, Finland, France, Germany, Indonesia, Italy, Korea, Malaysia, Netherlands, Poland, Portugal, Russia, Saudi Arabia, Senegal, Singapore, Slovakia, South Africa, Spain, Sweden, Switzerland, Taiwan, Turkey, Uganda, UK, and Vietnam.

Nationwide AlabamaCaliforniaFloridaGeorgiaIowaIllinoisIndianaKansasKentuckyLouisianaMassachusettsMarylandMichiganMinnesotaMissouriMississippiNorth CarolinaNebraskaNew JerseyNew York

Questions about this recall

Is EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology, Product Number recalled?

Yes. Covidien recalled EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology, Product Number on 9 Apr 2018. The recall is Class II and its status is Terminated. Recall number Z-1527-2018.

Why was it recalled?

There is a potential for improper welding of the yellow staple guide to the instrument. Use of a device with an improperly welded staple guide may result in improper staple formation potentially leading to bleeding or anastomotic leak.

Which lots are affected?

Lots: N7J1145MX, N7L0380MX, N7L0762MX, N7L1077MX, N7M0733MX,N7K0092MX, N7L0457MX, N7L0868MX, N7M0144MX, N7M0835MX, N7K0692MX, N7L0594MX, N7L0940MX, N7M0185MX N8A0144MX, N7K0693MX, N7L0676MX, N7L1076MX, N7M0732MX, N8A0166MX

Where was it sold?

Worldwide Distribution - US Nationwide in the US states of : AL, CA, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, NE, NJ, NY, OH, OR, SC, TN, TX, UT, and VA. The devices were distributed to the following foreign countries: UAE, Australia, Austria, Belgium, Bulgaria, Canada, Czech Republic, Denmark, Estonia, Finland, France, Germany, Indonesia, Italy, Korea, Malaysia, Netherlands, Poland, Portugal, Russia, Saudi Arabia, Senegal, Singapore, Slovakia, South Africa, Spain, Sweden, Switzerland, Taiwan, Turkey, Uganda, UK, and Vietnam.

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.

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