Recall Register

Food, drugs, devices › Coltene Whaledent Inc

Device recall: Dental pins - TMS LINK PLUS Self-Threading Pins - Product Usage: implanted into the teeth or for lab use for dental rest

FDA enforcement event 87645 · Class II · initiated 18 Mar 2021 · status Ongoing

DeviceVoluntary: Firm initiated1 product recordCuyahoga Falls, OH

FDA enforcement event 87645 is a device recall by Coltene Whaledent Inc of Cuyahoga Falls, OH, initiated 18 Mar 2021 and classified Class II, with 1 product record.

FDA defines Class II as a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. 89% of the 900 device enforcement events initiated in 2021 carry the same class.

Status: Ongoing. Initiation: voluntary: firm initiated. Coltene Whaledent Inc has 7 enforcement events on this register, with a median of 1 product record per event.

Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.

Recalling firm

Coltene Whaledent Inc, Cuyahoga Falls, OH.

Reason for recall

"The incorrect dental pins were packaged and subsequently distributed."

Distribution

"Worldwide distribution - US Nationwide distribution in the states of NJ, IN, NC, IL. GA, CA, NY, PA and the countries of Canada, Venezuela."

Product records

Recall numberProductQuantityClassStatusReport date
Z-1494-2021Dental pins - TMS LINK PLUS Self-Threading Pins - Product Usage: implanted into the teeth or for lab use for dental restoration purposes. The normal procedure requires a hole to be drilled into the tissue of a tooth with an intraoral drill prior to installation. Model number/Catalog number: L74165 packs of 20 pinsClass IIOngoing5 May 2021

Context

89%of 2021 device events are Class II900 events that year
1product record in this eventfirm median: 1
7events on this register for the firm

Other enforcement events for Coltene Whaledent Inc

InitiatedProduct (first record)TypeClassRecords
20 Jan 2023SciCan STATIS SL S10001 Dental Handpieces-Intended for the removal of carious material, reducing hard tooth structure, cDeviceClass II1
20 Oct 2020Alpen Clinic 100 Carbide Instruments (R100057C)DeviceClass II5
3 Jun 2020HYGENIC Dental Dam Forceps, Model no. H01262 - Product Usage: The dental dam forceps are intended to be used in conjunctDeviceClass II4
21 Aug 2018ParaPost Plus 25 Titanium Alloy Spiral Vented and Serrated Posts Catalog Number: P2845B Dental Posts are implanted into DeviceClass II1
13 Apr 2018Alpen Carbide 702 Cross Cut Tapered Fissure FG 10 pack (Carbide Burs), Model R100702 a rotary cutting device made from cDeviceClass II1
11 Dec 2013Latex Dental Dams labeled as Non-Latex Dental DamsDeviceClass II1

All 7 events for Coltene Whaledent Inc

Questions and answers

Why was this device recalled?

FDA's record gives the reason for recall as: "The incorrect dental pins were packaged and subsequently distributed."

What does Class II mean?

FDA classifies recalls by relative degree of health hazard. Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.

Where was the product distributed?

FDA's distribution pattern field reads: "Worldwide distribution - US Nationwide distribution in the states of NJ, IN, NC, IL. GA, CA, NY, PA and the countries of Canada, Venezuela."

Is the recall still ongoing?

FDA lists the status as Ongoing. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.

Where does this data come from?

openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.

Provenance

Source: openFDA device enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.