CLASS II ONGOING Device recall · Reported 24 Aug 2022 · FDA Enforcement Report
Polident Denture Cleansers recalled by Family Dollar Stores
Family Dollar Stores is recalling Polident Denture Cleansers, distributed nationwide in the US. The recall was initiated on 23 Jun 2022 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-1544-2022
- FDA event ID
- 90650
- Recalling firm
- Family Dollar Stores, Chesapeake, VA
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 23 Jun 2022
- FDA classified
- 17 Aug 2022
- Reported
- 24 Aug 2022
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Temperature Abuse
- Device type
- Dental Devices
Timeline
| 23 Jun 2022 | Recall initiated by company | |
| 17 Aug 2022 | Classified by FDA | +55 days |
| 24 Aug 2022 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Affected product was not appropriately stored in temperature-controlled areas between April 30, 2022 - June 10, 2022.
Foods that need refrigeration and were stored or shipped too warm can grow harmful bacteria without any change in look or smell.
Product as listed by the FDA
POLIDENT DENTURE CLEANSERS 84 CT, SKU 901634 POLIDENT DENTURE CLNS TAB 28CT, SKU 906131
Where it was distributed
Product distributed to Family Dollar retail stores in US nationwide.
Stores named: Dollar Tree
Questions about this recall
Why was it recalled?
Affected product was not appropriately stored in temperature-controlled areas between April 30, 2022 - June 10, 2022.
Which lots are affected?
All product sold between May 1, 2022 - June 10, 2022.
Where was it sold?
Product distributed to Family Dollar retail stores in US nationwide.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
21 other products · FDA event 90650This product is part of a recall event; the main page for the event is Ky Jelly Lubricant recalled by Family Dollar Stores.
More recalls from Family Dollar Stores
All 149| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Veriquick Pregnancy Test recalled by Family Dollar Stores | Family Dollar Stores | Temperature Abuse | 23 states |
| Device | CLASS II | Oral B Mouth Sore Rinse recalled by Family Dollar Stores | Family Dollar Stores | Temperature Abuse | 23 states |
| Device | CLASS II | Fixodent ORG Cream recalled by Family Dollar Stores | Family Dollar Stores | Temperature Abuse | 23 states |
| Device | CLASS II | At Home Marijuana Test Strip recalled by Family Dollar Stores | Family Dollar Stores | Temperature Abuse | 23 states |
| Device | CLASS II | Goodsense Denture Cleanser Grn Tab recalled by Family Dollar Stores | Family Dollar Stores | Temperature Abuse | 23 states |
Other Dental Devices recalls
All 426| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Grandio Universal Nano-Hybrid Restorative Material - Capsules 0.25Gm recalled | Henry Schein | Packaging Defects | Nationwide |
| Device | CLASS II | GM Helix Implant, Endosseous Dental Implant Article No. recalled | Straumann USA | Packaging Defects | Nationwide |
| Device | CLASS II | KL Owen Custom Orthodontic Solution recalled by Klowen Braces | Klowen Braces | Device Malfunction | Nationwide |
| Device | CLASS II | Straumann n!ce PMMA Full-arch Restoration recalled | Straumann USA | Other | 8 states |
| Device | CLASS II | Straumann n!ce Zr, HT, Full-arch Restoration recalled | Straumann USA | Other | 8 states |