IMPAK ACRYLIC RESIN LIQUID FOR BOTH IMPAK & IMPAK-PF POWDERS 1 qt — Class II medical device recall Z-1089-2016
Terminated recall by CMP Industries, Llc, reported 2016-03-16, distributed in MI, NJ, PA, TX. During the current inspection of CMP Industries, the FDA Investigator discovered that the firm had conducted a
| Recall number | Z-1089-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | CMP Industries, Llc, Albany, NY, United States |
| Recall initiated | 2013-11-18 |
| Classified | 2016-03-09 |
| Reported by FDA | 2016-03-16 |
| Terminated | 2018-05-23 |
| Distributed | MI, NJ, PA, TX |
| Countries outside the US | CA |
| Quantity | 246 units |
| Lot numbers | 103113 |
| Model numbers | 3306, 3748 |
Product
IMPAK ACRYLIC RESIN LIQUID FOR BOTH IMPAK & IMPAK-PF POWDERS 1 qt. size (946 cc), Part Number 3306, and 11 oz. size (325 cc), Part Number 3748. Indicated for relining a denture surface for repairing a fractured denture, or forming a new denture base.
Reason for recall
During the current inspection of CMP Industries, the FDA Investigator discovered that the firm had conducted a recall of Impak Acrylic Liquid Batch 103113 in 2013 due to potential rust without notifying the district.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1089-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.