Severity
Low
FDA Drug recall · Reported November 12, 2014
Failed Tablet/Capsule Specifications: Affected lot numbers may contain chipped or broken tablets.
Physicians Total Care, Inc. recalled Loratadine 24 HR-OTC,10 mg, 30-count bottle, Manufactured by Novartis Consumer Health, Pa… - a low-severity action.
Loratadine 24 HR-OTC,10 mg, 30-count bottle, Manufactured by Novartis Consumer Health, Pa… was recalled by Physicians Total Care, Inc. in November 12, 2014. Reason: Failed Tablet/Capsule Specifications: Affected lot numbers may contain chipped or broken tablets.. Check the official notice for the remedy. Verify recall #D-0239-2015 with the FDA Drug before acting.
The recall
Physicians Total Care, Inc. issued this low-severity FDA Drug recall-Failed Tablet/Capsule Specifications: Affected lot numbers may contain chipped or broken tablets..
Sourced from official FDA Drug enforcement records. Verify recall #D-0239-2015 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Drug action (record #D-0239-2015) was formally reported on November 12, 2014, with the manufacturer initiating the action on September 11, 2013. It is classified under Low severity (Class III), with a current status of Terminated. Physicians Total Care, Inc. is listed as the recalling firm, operating out of Tulsa, OK. Federal records list the affected scope as 7,740 pills.
The documented reason for this recall is: Failed Tablet/Capsule Specifications: Affected lot numbers may contain chipped or broken tablets. 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 low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Low
Affected scope
7,740 pills
Related Recalls
6
5 from same agency
Loratadine 24 HR-OTC,10 mg, 30-count bottle, Manufactured by Novartis Consumer Health, Parsippany, NJ 07054, Distributed by Physicians Total Care, Tulsa OK 74146, NDC 54868-5268-00
Failed Tablet/Capsule Specifications: Affected lot numbers may contain chipped or broken tablets.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | D-0239-2015 |
| Date reported | November 12, 2014 |
| Date initiated | September 11, 2013 |
| Recalling firm | Physicians Total Care, Inc. |
| Firm location | Tulsa, OK |
| Affected scope | 7,740 pills |
| 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 November 12, 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.