Severity
Low
LowClass IIITerminated
FDA Drug recall · Reported February 21, 2018
Klonopin (clonazepam) 0.5 mg Tablets,100-count bottle, Rx only. Made in Canada, Distributed by Genentech USA, Inc. A Member of the Roach Group, 1 DNA Way South San Francisco, CA 94080-4990. NDC 0004-0068-01
Labeling: Not Elsewhere Classified: Schedule IV controlled substance indicator of CIV being omitted from the product carton, primary label is correct.
Compiled from official public sources by the editorial team.
Verify with FDA Drug →
Genentech, Inc. recalled Klonopin (clonazepam) 0.5 mg Tablets,100-count bottle, Rx only. Made in Canada, Distribut… - a low-severity action.
Klonopin (clonazepam) 0.5 mg Tablets,100-count bottle, Rx only. Made in Canada, Distribut… was recalled by Genentech, Inc. in February 21, 2018. Reason: Labeling: Not Elsewhere Classified: Schedule IV controlled substance indicator of CIV being omitted from the…. Check the official notice for the remedy. Verify recall #D-0416-2018 with the FDA Drug before acting.
The recall
Genentech, Inc. issued this low-severity FDA Drug recall-Labeling: Not Elsewhere Classified: Schedule IV controlled substance indicator of CIV being omitted from the….
- Low
- severity level
- Class III
- classification
- February 21, 2018
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0416-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0416-2018) was formally reported on February 21, 2018, with the manufacturer initiating the action on February 5, 2018. It is classified under Low severity (Class III), with a current status of Terminated. Genentech, Inc. is listed as the recalling firm, operating out of South San Francisco, CA. Federal records list the affected scope as 3,192 bottles.
The documented reason for this recall is: Labeling: Not Elsewhere Classified: Schedule IV controlled substance indicator of CIV being omitted from the product carton, primary label is correct. Distribution data in the federal record shows the product reached: Distributed throughout the United States. 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 - 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.
Children & Baby Products recalls over time
Where this recall sits in its category - 3,731 children & baby products 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.
Affected scope
3,192 bottles
Related Recalls
6
0 from same agency
Product description
Klonopin (clonazepam) 0.5 mg Tablets,100-count bottle, Rx only. Made in Canada, Distributed by Genentech USA, Inc. A Member of the Roach Group, 1 DNA Way South San Francisco, CA 94080-4990. NDC 0004-0068-01
Reason for recall
Labeling: Not Elsewhere Classified: Schedule IV controlled substance indicator of CIV being omitted from the product carton, primary label is correct.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | D-0416-2018 |
| Date reported | February 21, 2018 |
| Date initiated | February 5, 2018 |
| Recalling firm | Genentech, Inc. |
| Firm location | South San Francisco, CA |
| Affected scope | 3,192 bottles |
| Distribution | Distributed throughout the United States |
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-0416-2018) 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? ▼
Klonopin (clonazepam) 0.5 mg Tablets,100-count bottle, Rx only. Made in Canada, Distributed by Genentech USA, Inc. A Member of the Roach Group, 1 DNA Way South San Francisco, CA 94080-4990. NDC 0004-0068-01. Recalled by Genentech, Inc.. Units affected: 3,192 bottles.
Why was this product recalled? ▼
Labeling: Not Elsewhere Classified: Schedule IV controlled substance indicator of CIV being omitted from the product carton, primary label is correct.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on February 21, 2018. Severity: Low. Recall number: D-0416-2018.
Where was the recalled product distributed? ▼
Distribution: Distributed throughout the United States.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-0416-2018) 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 February 21, 2018. 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.