Family Dollar marijuana test strips recalled over improper storage
Family Dollar recalled 329,044 at-home marijuana test strips (SKU 900752) due to improper storage outside labeled temperature requirements. Products were distributed across 22 states between June and October 2023.
The agency’s classification
FDA (Devices): Class II
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.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: FDA Class II recall for a storage compliance issue with no reported test failures, illnesses, or injuries. While improper storage may potentially affect test accuracy, the hazard remains theoretical and represents a product quality concern rather than a direct safety threat.
Plain-English summary
Family Dollar Stores is recalling approximately 329,044 At Home Marijuana Test Strips (SKU 900752). The products were stored outside of the manufacturer's labeled temperature requirements.
Storage at improper temperatures may affect the accuracy and reliability of test results. The recalled units were distributed to Family Dollar retail locations in 22 states between June 1, 2023 and October 4, 2023: Georgia, Alabama, Mississippi, Florida, Louisiana, Arkansas, Arizona, Kansas, Texas, Oklahoma, Colorado, New Mexico, Nebraska, Utah, Nevada, Wyoming, Idaho, South Dakota, North Dakota, California, Montana, Oregon, and Washington.
Consumers who have purchased this product should discontinue use.
The recalled product
- Product
- AT HOME MARIJUANA TEST STRIP, SKU 900752
- Manufacturer
- Family Dollar Stores, Llc.
- Category
- Medical Device — Test Kits
- Hazard
- Affected units
- 329,044
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (3)
- All units sold at stores between June 1
- 2023 and October 4
- 2023.
Distribution
Part of a larger recall action
This product is one of 10 recalled by Family Dollar Stores, Llc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 10 products in this recall →Related recalls
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