CLASS II ONGOING Drug recall · Reported 31 Aug 2022 · FDA Enforcement Report
Swan Povidone distributed to specific Family Dollar Stores recalled
Family Dollar Stores is recalling Swan Povidone distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022, 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
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-1410-2022
- FDA event ID
- 90566
- Recalling firm
- Family Dollar Stores, Chesapeake, VA
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 23 Jun 2022
- FDA classified
- 22 Aug 2022
- Reported
- 31 Aug 2022
- Type
- Voluntary: Firm initiated
- Customers notified by
- Other
- Reason category
- Manufacturing (CGMP) Deviations
Timeline
| 23 Jun 2022 | Recall initiated by company | |
| 22 Aug 2022 | Classified by FDA | +60 days |
| 31 Aug 2022 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
CGMP Deviations: product held outside appropriate storage temperature conditions.
Product as listed by the FDA
SWAN POVIDONE 4 FL OZ distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Where it was distributed
Nationwide within the United States
Stores named: Dollar Tree
Questions about this recall
Is Swan Povidone distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022 recalled?
Yes. Family Dollar Stores recalled Swan Povidone distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022 on 23 Jun 2022. The recall is Class II and its status is Ongoing. Recall number D-1410-2022.
Why was it recalled?
CGMP Deviations: product held outside appropriate storage temperature conditions.
Which lots are affected?
SKU: 999843
Where was it sold?
Nationwide within the United States
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
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 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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