CLASS III ONGOING Device recall · Reported 28 Dec 2022 · FDA Enforcement Report

Denticator Pick-a-dent, periodontal aid - intradental pick recalled

Young Dental Manufacturing I is recalling Denticator Pick-a-dent, periodontal aid - intradental pick, distributed nationwide in the US. The recall was initiated on 5 Dec 2022 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesLot 203257. Recall expanded on 12/19/2022 to include lot 207959

Quantity recalled600 packs

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-0725-2023
FDA event ID: 91173
Recalling firm: Young Dental Manufacturing I, Earth City, MO
Classification: Class III
Status: Ongoing
Recall initiated: 5 Dec 2022
FDA classified: 19 Dec 2022
Reported: 28 Dec 2022
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Labeling Errors
Device type: Dental Devices

Timeline

5 Dec 2022	Recall initiated by company
19 Dec 2022	Classified by FDA	+14 days
28 Dec 2022	Published in enforcement report	+9 days

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

Reason for recall

mislabeled product

Product as listed by the FDA

Denticator PICK-A-DENT, periodontal aid - intradental pick, REF 621714

Where it was distributed

Worldwide distribution - US Nationwide distribution in the states of IA, NY, PA, TN, TX, and the country of Canada.

Nationwide Iowa New York Pennsylvania Tennessee Texas

Questions about this recall

Why was it recalled?

mislabeled product

Which lots are affected?

Lot 203257. Recall expanded on 12/19/2022 to include lot 207959

Where was it sold?

Worldwide distribution - US Nationwide distribution in the states of IA, NY, PA, TN, TX, and the country of Canada.

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 III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

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.

More recalls from Young Dental Manufacturing I

All 5

Reported	Class	Recall	Company	Reason	Where
9 Oct 2024Device	CLASS II	Biotrol Purit Clean-It General Purpose Ultrasonic Cleaner recalled	Young Dental Manufacturing I	Packaging Defects	10 states
19 Jun 2024Device	CLASS II	Darby Prophylaxis Paste with 1.23% Fluoride Ion, Mint Coarse recalled	Young Dental Manufacturing I	Labeling Errors	Nationwide
15 Nov 2023Device	CLASS II	Contra Gray (soft) Turbo Plus Cups recalled	Young Dental Manufacturing I	Other	IN, MO, TN
14 Jun 2023Device	CLASS II	BencoDental iris 5% NaF varnish, White Mint recalled	Young Dental Manufacturing I	Packaging Defects	FL, NV, PA

Other Dental Devices recalls

All 426

Reported	Class	Recall	Company	Reason	Where
2 Sep 2026Device	CLASS II	Grandio Universal Nano-Hybrid Restorative Material - Capsules 0.25Gm recalled	Henry Schein	Packaging Defects	Nationwide
19 Aug 2026Device	CLASS II	GM Helix Implant, Endosseous Dental Implant Article No. recalled	Straumann USA	Packaging Defects	Nationwide
15 Jul 2026Device	CLASS II	KL Owen Custom Orthodontic Solution recalled by Klowen Braces	Klowen Braces	Device Malfunction	Nationwide
6 May 2026Device	CLASS II	Straumann n!ce PMMA Full-arch Restoration recalled	Straumann USA	Other	8 states
6 May 2026Device	CLASS II	Straumann n!ce Zr, HT, Full-arch Restoration recalled	Straumann USA	Other	8 states