Simply Saline Nasal Mist Recalled for Improper Storage Conditions
Simply Saline Nasal Mist 3.1 oz sold at Family Dollar stores has been recalled due to improper temperature storage between May and June 2022. Consumers should return the product to their local Family Dollar store.
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: This is a Class II medical device recall involving improper temperature storage of a nasal saline product. Although no illnesses or injuries have been reported, improper storage of sterile medical devices poses an inherent risk that meets the criterion of risk-of-harm products where injury has not yet been reported.
Plain-English summary
Simply Saline Nasal Mist 3.1 oz, SKU 999801, manufactured by Family Dollar Stores, LLC, has been recalled.
The affected product was not stored in temperature-controlled areas between April 30, 2022, and June 10, 2022. All units sold at Family Dollar retail locations nationwide during May 1 through June 10, 2022, are included in this recall.
Consumers who purchased this nasal mist should return it to their local Family Dollar store. The FDA has classified this as a Class II recall.
The recalled product
- Product
- SIMPLY SALINE NASAL MIST 3.1 OZ, SKU 999801
- Manufacturer
- Family Dollar Stores, Llc.
- Category
- Medical Device — Nasal Care
- 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