Contact Lens Multi-Purpose Solution Recalled for Improper Storage
Family Dollar is recalling BIOTRU Multi-Purpose Solution (4 oz, SKU 999009) due to improper temperature-controlled storage. Approximately 1,051 units were affected across US Family Dollar stores.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: FDA Class II recall for contact lens solution with improper storage. No illnesses or injuries reported; hazard is theoretical but significant for eye-contact products.
Plain-English summary
Family Dollar Stores, LLC is recalling BIOTRU Multi-Purpose Solution (4 oz, SKU 999009). Approximately 1,051 units were distributed to Family Dollar retail stores nationwide, sold between May 1, 2022 and June 10, 2022.
The product was not appropriately stored in temperature-controlled areas between April 30, 2022 and June 10, 2022. This storage failure prompted the FDA to classify the recall as a Class II issue.
Consumers who obtained this product should stop using it and dispose of it.
The recalled product
- Product
- B L BIOTRU MULTI PURPOSE SOLUTION 4 FLOZ, SKU 999009
- Manufacturer
- Family Dollar Stores, Llc.
- Hazard
- improper-storage
- temperature-excursion
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 product sold between May 1
- 2022 - June 10
- 2022.
Distribution
Distributed nationwide across the United States.
Related recalls
Same category
- SevereMedline Spinal Block Kits Recalled for Data Integrity and Efficacy Issues
FDA (Devices) · 2026-06-03
- SevereAbiomed Automated Impella Controller recalled for motor control and pump failure risks
FDA (Devices) · 2026-06-03
- HighGE APEXPRO and CARESCAPE Telemetry Systems Risk Loss of Patient Monitoring
FDA (Devices) · 2026-06-03
- CriticalMedline spinal anesthetic kits recalled for quality and efficacy concerns
FDA (Devices) · 2026-06-03
- SevereMedline spinal anesthesia kits recalled for bupivacaine quality issues
FDA (Devices) · 2026-06-03