Severity
Moderate
ModerateClass IITerminated
FDA Drug recall · Reported October 29, 2014
ZEE Aspirin 325mg - 24 tablets in single dose packets, OTC, Manufactured for ZEE Medical Inc., Irvine,CA 92606 by ULTRA Tab Laboratories, Inc. Highland, NY 12528
Incorrect/Undeclared Excipients: ZEE Medical is recalling ZEE Aspirin due to the incorrect listing of inactive ingredients on the product label.
Zee Medical Products Inc recalled ZEE Aspirin 325mg - 24 tablets in single dose packets, OTC, Manufactured for ZEE Medical … - a moderate-severity action.
ZEE Aspirin 325mg - 24 tablets in single dose packets, OTC, Manufactured for ZEE Medical … was recalled by Zee Medical Products Inc in October 29, 2014. Reason: Incorrect/Undeclared Excipients: ZEE Medical is recalling ZEE Aspirin due to the incorrect listing of inactiv…. Check the official notice for the remedy. Verify recall #D-0041-2015 with the FDA Drug before acting.
The recall
Zee Medical Products Inc issued this moderate-severity FDA Drug recall-Incorrect/Undeclared Excipients: ZEE Medical is recalling ZEE Aspirin due to the incorrect listing of inactiv….
- Moderate
- severity level
- Class II
- classification
- October 29, 2014
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0041-2015 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0041-2015) was formally reported on October 29, 2014, with the manufacturer initiating the action on October 7, 2014. It is classified under Moderate severity (Class II), with a current status of Terminated. Zee Medical Products Inc is listed as the recalling firm, operating out of Irvine, CA. Federal records list the affected scope as 43,752 boxes.
The documented reason for this recall is: Incorrect/Undeclared Excipients: ZEE Medical is recalling ZEE Aspirin due to the incorrect listing of inactive ingredients on the product label. Distribution data in the federal record shows the product reached: Nationwide in US. 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
43,752 boxes
Related Recalls
6
5 from same agency
Product description
ZEE Aspirin 325mg - 24 tablets in single dose packets, OTC, Manufactured for ZEE Medical Inc., Irvine,CA 92606 by ULTRA Tab Laboratories, Inc. Highland, NY 12528
Reason for recall
Incorrect/Undeclared Excipients: ZEE Medical is recalling ZEE Aspirin due to the incorrect listing of inactive ingredients on the product label.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | D-0041-2015 |
| Date reported | October 29, 2014 |
| Date initiated | October 7, 2014 |
| Recalling firm | Zee Medical Products Inc |
| Firm location | Irvine, CA |
| Affected scope | 43,752 boxes |
| Distribution | Nationwide in US |
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-0041-2015) 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? ▼
ZEE Aspirin 325mg - 24 tablets in single dose packets, OTC, Manufactured for ZEE Medical Inc., Irvine,CA 92606 by ULTRA Tab Laboratories, Inc. Highland, NY 12528. Recalled by Zee Medical Products Inc. Units affected: 43,752 boxes.
Why was this product recalled? ▼
Incorrect/Undeclared Excipients: ZEE Medical is recalling ZEE Aspirin due to the incorrect listing of inactive ingredients on the product label.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on October 29, 2014. Severity: Moderate. Recall number: D-0041-2015.
Where was the recalled product distributed? ▼
Distribution: Nationwide in US.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-0041-2015) 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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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 October 29, 2014. 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.