Severity
Low
FDA Drug recall · Reported April 21, 2021
Failed Stability Specifications: product did not meet viscosity results.
Teligent Pharma, Inc. recalled Lidocaine Ointment USP, 5%, NET WT 35.44 g (1 1/4 Oz) tube, Rx Only, Teligent Pharma Inc.… - a low-severity action.
Lidocaine Ointment USP, 5%, NET WT 35.44 g (1 1/4 Oz) tube, Rx Only, Teligent Pharma Inc.… was recalled by Teligent Pharma, Inc. in April 21, 2021. Reason: Failed Stability Specifications: product did not meet viscosity results.. Check the official notice for the remedy. Verify recall #D-0331-2021 with the FDA Drug before acting.
The recall
Teligent Pharma, Inc. issued this low-severity FDA Drug recall-Failed Stability Specifications: product did not meet viscosity results..
Sourced from official FDA Drug enforcement records. Verify recall #D-0331-2021 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Drug action (record #D-0331-2021) was formally reported on April 21, 2021, with the manufacturer initiating the action on March 29, 2021. It is classified under Low severity (Class III), with a current status of Terminated. Teligent Pharma, Inc. is listed as the recalling firm, operating out of Buena, NJ. Federal records list the affected scope as 62,040 tubes.
The documented reason for this recall is: Failed Stability Specifications: product did not meet viscosity results. Distribution data in the federal record shows the product reached: Nationwide in the USA. 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
62,040 tubes
Related Recalls
6
5 from same agency
Lidocaine Ointment USP, 5%, NET WT 35.44 g (1 1/4 Oz) tube, Rx Only, Teligent Pharma Inc., Buena, New Jersey, 08310, NDC 52565-008-14.
Failed Stability Specifications: product did not meet viscosity results.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | D-0331-2021 |
| Date reported | April 21, 2021 |
| Date initiated | March 29, 2021 |
| Recalling firm | Teligent Pharma, Inc. |
| Firm location | Buena, NJ |
| Affected scope | 62,040 tubes |
| Distribution | Nationwide in the USA |
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 April 21, 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.