Contact Lens Solution Recalled for Improper Temperature Storage
OPTI FREE REPLENISH contact lens solution sold at Family Dollar stores (May 1–June 10, 2022) was not stored in temperature-controlled areas and is being recalled.
What this means for you
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: This is a Class II medical device recall with no reported illnesses or injuries. The hazard is improper storage of contact lens solutions, which represents a precautionary recall. Per the rubric, precautionary recalls without reported adverse events receive a Moderate rating.
Plain-English summary
OPTI FREE REPLENISH MULTI PURPOSE 2 OZ contact lens solution is being recalled. The product was distributed to Family Dollar retail stores nationwide and was sold between May 1, 2022 and June 10, 2022.
The recall was initiated because the affected product was not appropriately stored in temperature-controlled areas between April 30, 2022 and June 10, 2022. Proper temperature control is critical for maintaining the safety and effectiveness of contact lens care solutions.
The recalled product
- Product
- OPTI FREE REPLENISH MULTI PURPOSE 2 OZ
- Manufacturer
- Family Dollar Stores, Llc.
- Hazard
- improper-storage
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