Severity
Moderate
ModerateClass IITerminated
FDA Drug recall · Reported January 12, 2022
Cefixime 400 mg capsule, packaged in a) 2-count bottle (NDC 70518-2749-02), b) 2-count blister pack (NDC 70518-2749-03), Rx only, MFG: Ascend Labs, LLC, Montvale, NJ 07645
Failed Impurities/Degradation Specifications
Compiled from official public sources by the editorial team.
Verify with FDA Drug →
RemedyRepack Inc. recalled Cefixime 400 mg capsule, packaged in a) 2-count bottle (NDC 70518-2749-02), b) 2-count bl… - a moderate-severity action.
Cefixime 400 mg capsule, packaged in a) 2-count bottle (NDC 70518-2749-02), b) 2-count bl… was recalled by RemedyRepack Inc. in January 12, 2022. Reason: Failed Impurities/Degradation Specifications. Check the official notice for the remedy. Verify recall #D-0360-2022 with the FDA Drug before acting.
The recall
RemedyRepack Inc. issued this moderate-severity FDA Drug recall-Failed Impurities/Degradation Specifications.
- Moderate
- severity level
- Class II
- classification
- January 12, 2022
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0360-2022 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0360-2022) was formally reported on January 12, 2022, with the manufacturer initiating the action on December 29, 2021. It is classified under Moderate severity (Class II), with a current status of Terminated. RemedyRepack Inc. is listed as the recalling firm, operating out of Indiana, PA. Federal records list the affected scope as a) 716 bottles/ 1432 capsules b) 223 blister packs/ 466 capsules.
The documented reason for this recall is: Failed Impurities/Degradation Specifications Distribution data in the federal record shows the product reached: Product was distributed to two direct accounts in MI and PA.. 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.
Drugs & Medications recalls over time
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.
Affected scope
a) 716 bottles/ 1432 capsules b) 223 blister packs/ 466 capsules
Related Recalls
6
5 from same agency
Product description
Cefixime 400 mg capsule, packaged in a) 2-count bottle (NDC 70518-2749-02), b) 2-count blister pack (NDC 70518-2749-03), Rx only, MFG: Ascend Labs, LLC, Montvale, NJ 07645
Reason for recall
Failed Impurities/Degradation Specifications
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | D-0360-2022 |
| Date reported | January 12, 2022 |
| Date initiated | December 29, 2021 |
| Recalling firm | RemedyRepack Inc. |
| Firm location | Indiana, PA |
| Affected scope | a) 716 bottles/ 1432 capsules b) 223 blister packs/ 466 capsules |
| Distribution | Product was distributed to two direct accounts in MI and PA. |
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.
- Check the recall number (D-0360-2022) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
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.
Frequently Asked Questions
What product was recalled? ▼
Cefixime 400 mg capsule, packaged in a) 2-count bottle (NDC 70518-2749-02), b) 2-count blister pack (NDC 70518-2749-03), Rx only, MFG: Ascend Labs, LLC, Montvale, NJ 07645. Recalled by RemedyRepack Inc.. Units affected: a) 716 bottles/ 1432 capsules b) 223 blister packs/ 466 capsules.
Why was this product recalled? ▼
Failed Impurities/Degradation Specifications
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on January 12, 2022. Severity: Moderate. Recall number: D-0360-2022.
Where was the recalled product distributed? ▼
Distribution: Product was distributed to two direct accounts in MI and PA..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-0360-2022) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Compare this recall with PRED MILD, prednisolone acetate ophthalmic suspension, USP,… →
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 12, 2022. 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.