FindMyRecallSubscribe
Class II: temporary or reversible health riskOngoing

Family Dollar Stores Dayquil Cold Flu Lqd 12 Fl Oz Sku 900205 Ric Recall

DAYQUIL COLD FLU LQD 12 FL OZ SKU 900205 RIC NIGHT TIME CLD FLU RLF SOFT GELS 8 CT SK…

Family Dollar Stores, Llc. · Chesapeake, VA

Risk level
Class II
Reported by FDA
Aug 31, 2022
Recall ID
D-1454-2022
Check your lot numberHow we source this data

Summary

Family Dollar Stores recalled Dayquil Cold Flu Lqd 12 Fl Oz Sku 900205 Ric starting Jun 23, 2022. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-1454-2022 on Aug 31, 2022. Reason: CGMP Deviations: product held outside appropriate storage temperature conditions. Status: Ongoing.

Why it was recalled

CGMP Deviations: product held outside appropriate storage temperature conditions.

Product description

DAYQUIL COLD FLU LQD 12 FL OZ SKU 900205 RIC NIGHT TIME CLD FLU RLF SOFT GELS 8 CT SKU 900523 ALKA SELTZER PLUS DAY NIGHT LGEL 20 CT SKU 902012 GS COLD FLU RELIEF NGHTTIME CHRY12FL OZ SKU 917523 RIC COLD FLU DAY TIME LIQUID CAP 16 CT SKU 903037 ASP SEVERE COLD COUGH CITRUS 20CT SKU 902906 ASP SEVERE COLD ORANGE ZEST 20CT SKU 902908 ALKA SELTZER PLUS SEVERE COLD ORIG 20CT SKU 903333 AS PLUS SINUS ALLERGY N COUGH PMAX 16CT SKU 903335 NYQUIL SEVERE VAPOCOOL LIQUID 8 FL OZ SKU 999542 AS PLUS MAX STRNGTH SINUS CONG N PN 20CT SKU 903334 GS DAYTIME COLD FLU RLF ORANGE 12FL OZ SKU 900576 NYQUIL SEVERE COLD FLU BERRY 8 FL OZ SKU 903759 NYQUIL ORGNL COLD AND FLU LQD 12FL OZ SKU 900207 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.

Lot numbers, UPCs & expiration codes

SKUs: 900205; 900523; 902012; 917523; 903037; 902906; 902908; 903333; 903335; 999542; 903334; 900576; 903759; 900207

Where it was sold

Nationwide within the United States

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-1454-2022
Classification
Class II
Status
Ongoing
Recall initiated
Jun 23, 2022
FDA report date
Aug 31, 2022
Quantity
Unknown
Recall type
Voluntary: Firm initiated
Recalling firm
Family Dollar Stores, Llc.

Original FDA data

Every field from FDA enforcement report D-1454-2022, exactly as published.

Show all FDA fields
City
Chesapeake
State
VA
Status
Ongoing
Country
United States
Event ID
90566
Address
500 Volvo Pkwy
Code information
SKUs: 900205; 900523; 902012; 917523; 903037; 902906; 902908; 903333; 903335; 999542; 903334; 900576; 903759; 900207
Postal code
23320-1604
Report date
Aug 31, 2022
Product type
Drugs
Recall number
D-1454-2022
Classification
Class II
Recalling firm
Family Dollar Stores, Llc.
Product quantity
Unknown
Reason for recall
CGMP Deviations: product held outside appropriate storage temperature conditions.
Voluntary / mandated
Voluntary: Firm initiated
Product description
DAYQUIL COLD FLU LQD 12 FL OZ SKU 900205 RIC NIGHT TIME CLD FLU RLF SOFT GELS 8 CT SKU 900523 ALKA SELTZER PLUS DAY NIGHT LGEL 20 CT SKU 902012 GS COLD FLU RELIEF NGHTTIME CHRY12FL OZ SKU 917523 RIC COLD FLU DAY TIME LIQUID CAP 16 CT SKU 903037 ASP SEVERE COLD COUGH CITRUS 20CT SKU 902906 ASP SEVERE COLD ORANGE ZEST 20CT SKU 902908 ALKA SELTZER PLUS SEVERE COLD ORIG 20CT SKU 903333 AS PLUS SINUS ALLERGY N COUGH PMAX 16CT SKU 903335 NYQUIL SEVERE VAPOCOOL LIQUID 8 FL OZ SKU 999542 AS PLUS MAX STRNGTH SINUS CONG N PN 20CT SKU 903334 GS DAYTIME COLD FLU RLF ORANGE 12FL OZ SKU 900576 NYQUIL SEVERE COLD FLU BERRY 8 FL OZ SKU 903759 NYQUIL ORGNL COLD AND FLU LQD 12FL OZ SKU 900207 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.
Distribution pattern
Nationwide within the United States
Recall initiation date
Jun 23, 2022
Initial firm notification
Other
Center classification date
Aug 22, 2022

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1454-2022, published Aug 31, 2022. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

How we source and update recall data · Report incorrect information

Other recent drug recalls