CLASS II Drug recall · Reported 29 Jan 2014 · FDA Enforcement Report
Carvedilol Phosphate ER, Capsule, 20 mg recalled by Aidapak Services
Aidapak Services is recalling Carvedilol Phosphate ER, Capsule, 20 mg, distributed in Arizona, California, Oregon, Washington. The recall was initiated on 2 Jul 2013 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-777-2014
- FDA event ID
- 65690
- Recalling firm
- Aidapak Services, Vancouver, WA
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 2 Jul 2013
- FDA classified
- 20 Jan 2014
- Reported
- 29 Jan 2014
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Labeling Errors
- Drug class
- Blood Pressure Medication
Timeline
| 2 Jul 2013 | Recall initiated by company | |
| 20 Jan 2014 | Classified by FDA | +202 days |
| 29 Jan 2014 | 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
Labeling: Label Mixup: CARVEDILOL PHOSPHATE ER, Capsule, 20 mg may be potentially mislabeled as the following drug: BUMETANIDE, Tablet, 1 mg, NDC 00093423301, Pedigree: W003224, EXP: 6/17/2014.
Product as listed by the FDA
CARVEDILOL PHOSPHATE ER, Capsule, 20 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00007337113.
Where it was distributed
Repacked drugs were distributed in Arizona, California, Oregon, and Washington.
Questions about this recall
Is Carvedilol Phosphate ER, Capsule, 20 mg recalled?
Yes. Aidapak Services recalled Carvedilol Phosphate ER, Capsule, 20 mg on 2 Jul 2013. The recall is Class II and its status is Terminated. Recall number D-777-2014.
Why was it recalled?
Labeling: Label Mixup: CARVEDILOL PHOSPHATE ER, Capsule, 20 mg may be potentially mislabeled as the following drug: BUMETANIDE, Tablet, 1 mg, NDC 00093423301, Pedigree: W003224, EXP: 6/17/2014.
Which lots are affected?
CARVEDILOL PHOSPHATE ER, Capsule, 20 mg has the following codes: Pedigree: W003225, EXP: 6/17/2014.
Where was it sold?
Repacked drugs were distributed in Arizona, California, Oregon, and Washington.
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.
More recalls from Aidapak Services
All 538| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | MERCapsuleTOPURINE, Tablet, 50 mg recalled by Aidapak Services | Aidapak Services | Labeling Errors | 4 states |
| Drug | CLASS II | Selenium, Tablet, 50 mcg, Over The Counter recalled by Aidapak Services | Aidapak Services | Labeling Errors | 4 states |
| Drug | CLASS II | Venlafaxine HCL, Tablet, 100 mg recalled by Aidapak Services | Aidapak Services | Labeling Errors | 4 states |
| Drug | CLASS II | Ascorbic Acid, Tablet, 500 mg, Over The Counter recalled | Aidapak Services | Labeling Errors | 4 states |
| Drug | CLASS II | Calcitriol, Capsule, 25 mcg recalled by Aidapak Services | Aidapak Services | Packaging Defects | 4 states |