Recall Record

Gibbstown, NJ, United States

Keystone Industries recalls

6 recalls recorded since 2018, most recently on 21 May 2026. 5 are listed as ongoing. Status and classification are as published by the FDA.

Recalls6
Ongoing (FDA)5
Terminated or completed1
Class I (FDA)0

Ongoing Class II Drugs

Recall started
21 May 2026
Reason
Defective container:may contain bottles with incomplete seals
Distribution
Nationwide in the USA
Initiated
Voluntary: Firm initiated
Recall numbers
D-0602-2026, D-0605-2026, D-0601-2026, D-0603-2026, D-0604-2026, D-0606-2026, D-0600-2026

Terminated Class II Drugs

Recall started
14 November 2024
Terminated
23 April 2026
Reason
CGMP deviations: the bulk product was rejected by the Quality Unit after routine inspection of the mixing vessel showed scratches on the sides and bottom of the mixing vessel. Product was to be rejected but was inadvertently released and shipped to customers.
Distribution
Nationwide in the USA and Canada, Dominican Republic, El Salvador, Honduras, and Qatar.
Initiated
Voluntary: Firm initiated
Recall numbers
D-0137-2025, D-0148-2025, D-0146-2025, D-0145-2025, D-0140-2025, D-0142-2025, D-0139-2025, D-0144-2025, D-0138-2025, D-0147-2025, D-0143-2025, D-0141-2025

Ongoing Class II Drugs

Recall started
17 October 2024
Reason
Subpotent Drug
Distribution
Nationwide within the United States
Initiated
Voluntary: Firm initiated
Recall number
D-0046-2025

Ongoing Class II Medical devices

Recall started
20 November 2023
Reason
Keyprint Keysplint Hard Clear 1 kg resin bottles were inadvertently packaged with the wrong Instructions for Use. Keysplint Hard Clear were placed inside a zip lock bag along with KeySplint Soft Instructions for Use (IFU).
Distribution
Worldwide distribution - US Nationwide and the country of China.
Initiated
Voluntary: Firm initiated
Recall number
Z-0630-2024

Ongoing Class II Medical devices

Recall started
21 July 2023
Reason
A bottle of Copaliner Solvent was inadvertently packaged into a box labeled as Copaliner Varnish (0921526) and sold as Copaliner Varnish (0921526).
Distribution
Worldwide distribution - US Nationwide and the countries of Canada, Bangladesh, Germany, UK.
Initiated
Voluntary: Firm initiated
Recall number
Z-2579-2023

Ongoing Class II Medical devices

Recall started
10 April 2023
Reason
The Hard Line Chairside Reline Kit (570-0718) (0921940HS) was labeled as Soft Line Chairside Reline Kit (570-0717) (0921250HS) on the outer box. The contents of the Kit and the IFU enclosed with the kit were correctly labeled as Hard Line materials
Distribution
US Nationwide distribution in the states of IL, PA, FL NV, TX.
Initiated
Voluntary: Firm initiated
Recall number
Z-2580-2023

A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.