CellCept (mycophenolate mofetil) capsules, 250 mg, packaged in a) 12 x 120-count bottles per carton, NDC 0004-0259-05; b) 120-count capsules per bottle, NDC 0004-0259-51; Made in Ireland; Distributed by: Genentech USA, Inc., South San Francisco, CA 94080.

Short Fill: some bottles contained less than 120-count per labeled claim.

Recall #: D-097-2013
Affected scope: 1128 bottles
Initiated: September 27, 2012

Compiled from official public sources by the publisher. · Updated September 2026

Genentech, Inc. recalled CellCept (mycophenolate mofetil) capsules, 250 mg, packaged in a) 12 x 120-count bottles … - a low-severity action.

CellCept (mycophenolate mofetil) capsules, 250 mg, packaged in a) 12 x 120-count bottles … was recalled by Genentech, Inc. in December 26, 2012. Reason: Short Fill: some bottles contained less than 120-count per labeled claim.. Check the official notice for the remedy. Verify recall #D-097-2013 with the FDA Drug before acting.

The recall

Genentech, Inc. issued this low-severity FDA Drug recall-Short Fill: some bottles contained less than 120-count per labeled claim..

Low
severity level: Class III
classification: December 26, 2012
reported

Sourced from official FDA Drug enforcement records. Verify recall #D-097-2013 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) 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, 1 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 agency-classified recall sits among FDA Class I/II/III notices

Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. 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.

Product description

CellCept (mycophenolate mofetil) capsules, 250 mg, packaged in a) 12 x 120-count bottles per carton, NDC 0004-0259-05; b) 120-count capsules per bottle, NDC 0004-0259-51; Made in Ireland; Distributed by: Genentech USA, Inc., South San Francisco, CA 94080.

Reason for recall

Short Fill: some bottles contained less than 120-count per labeled claim.

Recall Profile

Structured summary of the FDA Drug recall record
Attribute	Value
Agency	U.S. Food and Drug Administration
Severity class	Low (Class III)
Status	Terminated
Recall number	D-097-2013
Date reported	December 26, 2012
Date initiated	September 27, 2012
Recalling firm	Genentech, Inc.
Firm location	South San Francisco, CA
Affected scope	1128 bottles
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.

Check the recall number (D-097-2013) 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? ▼

Why was this product recalled? ▼

Short Fill: some bottles contained less than 120-count per labeled claim.

Which agency issued this recall? ▼

This recall was issued by the FDA Drug on December 26, 2012. Severity: Low. Recall number: D-097-2013.

Where was the recalled product distributed? ▼

Distribution: Nationwide.

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.

Nationwide recalls with similar severity or category timing

Drug and device notices outside this firm and state, matched by severity timing and product category.

Similar severity · nearest report date

Same archive severity grade (Low), closest by report date among other firms and states.

Choletec - Kit for the Preparation of Tec… 2012-12-26 Clean & Clear advantage, 3-in-1 foaming w… 2012-12-26 Garden Fresh Gourmet Nacho Cheese Tortill… 2012-12-26 El Matador Mexican Style Salted Tortilla … 2012-12-26

Similar Children & Baby Products · nearest report date

Same product category, closest by report date among other firms and states (deduped against the severity set).

Four Retailers Agree to Stop Sale and Vol… 2012-12-27 Meijer Recalls Falls Creek Kids Denim Jea… 2012-12-27 Ella's Kitchen yum yummy milk + vanilla b… 2012-12-19 Ella's Kitchen yum yummy apple + ginger b… 2012-12-19

Compare this recall with CLEAR EYES Maximum Itchy Eye Relief, 0.5 fl oz (15 mL) per … → · All Children & Baby Products recalls

This recall: FDA Drug, reported December 26, 2012. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026