CLASS II Device recall · Reported 12 Jun 2019 · FDA Enforcement Report

Sterile Nail Nipper, Barrel Spring (I68400), Sterile recalled

Centurion Medical Products is recalling Sterile Nail Nipper, Barrel Spring (I68400), Sterile, distributed nationwide in the US. The recall was initiated on 29 Mar 2019 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot 2018121101, exp 2023-11-30

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-1720-2019
FDA event ID: 82667
Recalling firm: Centurion Medical Products, Williamston, MI
Classification: Class II
Status: Terminated
Recall initiated: 29 Mar 2019
FDA classified: 4 Jun 2019
Reported: 12 Jun 2019
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Sterility
Device type: Masks, Gloves & PPE

Timeline

29 Mar 2019	Recall initiated by company
4 Jun 2019	Classified by FDA	+67 days
12 Jun 2019	Published in enforcement report	+8 days

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

Reason for recall

Compromised seal on the sterile barrier pouch.

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

Sterile Nail Nipper, Barrel Spring (I68400), Sterile

Where it was distributed

US nationwide distribution.

Nationwide

Questions about this recall

Why was it recalled?

Compromised seal on the sterile barrier pouch.

Which lots are affected?

Lot 2018121101, exp 2023-11-30

Where was it sold?

US nationwide distribution.

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 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

1 other product · FDA event 82667

This product is part of a recall event; the main page for the event is Sterile Nail Clipper Concave Edge (67710) recalled.

Reported	Class	Recall	Company	Reason	Where
12 Jun 2019	CLASS II	Sterile Nail Clipper Concave Edge (67710) recalled	Centurion Medical Products	Sterility	Nationwide

More recalls from Centurion Medical Products

All 152

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15 Jul 2020Device	CLASS II	Centurion Difficult IV KIT containing BD's Vacutainer recalled	Centurion Medical Products	Foreign Material	Nationwide
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Other Masks, Gloves & PPE recalls

All 447

Reported	Class	Recall	Company	Reason	Where
29 Jul 2026Device	CLASS II	P28 Phanton Intramedullary Nail System recalled by Paragon 28	Paragon 28	Sterility	Nationwide
8 Jul 2026Device	CLASS II	Cyberknife Treatment Deliver System equipped recalled	Accuray	Device Malfunction	Nationwide
8 Jul 2026Device	CLASS II	Adapter for Head Positioning recalled by Baxter Healthcare	Baxter Healthcare	Other	Nationwide
8 Jul 2026Device	CLASS II	Cyberknife Treatment Deliver System equipped recalled	Accuray	Device Malfunction	Nationwide
3 Jun 2026Device	CLASS II	Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference recalled	O&M Halyard	Other	Nationwide