SPICE — Class II medical device recall Z-1701-2020
Terminated recall by Carolina Liquid Chemistries Corp, reported 2020-04-22, distributed in AL, CA, LA, NY. Corrections are being made to the device labeling regarding its intended use, to include a statement clarifyin
| Recall number | Z-1701-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Carolina Liquid Chemistries Corp, Brea, CA, United States |
| Recall initiated | 2020-02-10 |
| Classified | 2020-04-10 |
| Reported by FDA | 2020-04-22 |
| Terminated | 2021-01-14 |
| Distributed | AL, CA, LA, NY |
| Reason classes | labeling |
| Lot numbers | D1906, D1939 |
Product
SPICE (JWH-018) CC443
Reason for recall
Corrections are being made to the device labeling regarding its intended use, to include a statement clarifying it is for research purposes only.
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-1701-2020. 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.