Severity
Moderate
FDA Drug recall · Reported January 6, 2021
Failed Impurity/Degradation Specifications
Ascend Laboratories LLC recalled Ascend Laboratories, llc Cephalexin for Oral Suspension, USP 250 mg per 5 mL 100 ml (when… - a moderate-severity action.
Ascend Laboratories, llc Cephalexin for Oral Suspension, USP 250 mg per 5 mL 100 ml (when… was recalled by Ascend Laboratories LLC in January 6, 2021. Reason: Failed Impurity/Degradation Specifications. Check the official notice for the remedy. Verify recall #D-0178-2021 with the FDA Drug before acting.
The recall
Ascend Laboratories LLC issued this moderate-severity FDA Drug recall-Failed Impurity/Degradation Specifications.
Sourced from official FDA Drug enforcement records. Verify recall #D-0178-2021 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Drug action (record #D-0178-2021) was formally reported on January 6, 2021, with the manufacturer initiating the action on December 17, 2020. It is classified under Moderate severity (Class II), with a current status of Terminated. Ascend Laboratories LLC is listed as the recalling firm, operating out of Parsippany, NJ. Federal records list the affected scope as 29,317 bottles.
The documented reason for this recall is: Failed Impurity/Degradation Specifications Distribution data in the federal record shows the product reached: Nationwide. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 5 from FDA Drug - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 14,287 drugs & medications recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Moderate
Affected scope
29,317 bottles
Related Recalls
6
5 from same agency
Ascend Laboratories, llc Cephalexin for Oral Suspension, USP 250 mg per 5 mL 100 ml (when mixed) Rx Only Manufactured by: Alkem Laboratories, Ltd, Mumbai -400 013 INDIA Distributed by: Ascend Laboratories, LLC Parsippany, NJ 07054 NDC 67877-545-88
Failed Impurity/Degradation Specifications
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | D-0178-2021 |
| Date reported | January 6, 2021 |
| Date initiated | December 17, 2020 |
| Recalling firm | Ascend Laboratories LLC |
| Firm location | Parsippany, NJ |
| Affected scope | 29,317 bottles |
| Distribution | Nationwide |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported January 6, 2021. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.