Severity
Critical
CriticalClass ITerminated
FDA Devices recall · Reported January 29, 2014
TRUFILL¿ n-Butyl Cyanoacrylate (n-BCA) Liquid Embolic System; Two 1 g tubes of n-BCA, one 10 mL vial of Ethiodized Oil and one 1 g vial of Tantalum Powder Product Code: 631-400; The TRUFILL n-BCA Liquid Embolic System is indicated for the embolization of cerebral arteriovenous malformations (AVMs) when pre-surgical devascularization is desired.
Incorrect instructions for use (IFU).
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Codman & Shurtleff, Inc. recalled TRUFILL¿ n-Butyl Cyanoacrylate (n-BCA) Liquid Embolic System; Two 1 g tubes of n-BCA, on… - a critical-severity action.
TRUFILL¿ n-Butyl Cyanoacrylate (n-BCA) Liquid Embolic System; Two 1 g tubes of n-BCA, on… was recalled by Codman & Shurtleff, Inc. in January 29, 2014. Reason: Incorrect instructions for use (IFU).. Check the official notice for the remedy. Verify recall #Z-0788-2014 with the FDA Devices before acting.
The recall
Codman & Shurtleff, Inc. issued this critical-severity FDA Devices recall-Incorrect instructions for use (IFU)..
- Critical
- severity level
- 4K units
- affected scope
- Class I
- classification
- January 29, 2014
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0788-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0788-2014) was formally reported on January 29, 2014, with the manufacturer initiating the action on October 11, 2013. It is classified under Critical severity (Class I), with a current status of Terminated. Codman & Shurtleff, Inc. is listed as the recalling firm, operating out of Raynham, MA. Federal records list the affected scope as 3,860.
The documented reason for this recall is: Incorrect instructions for use (IFU). Distribution data in the federal record shows the product reached: Worldwide Distribution: US (nationwide) including Puerto Rico; and internationally to: Costa Rica and Russia.. 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, 3 from FDA Devices - 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.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices 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 high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
3,860
Related Recalls
6
3 from same agency
Product description
TRUFILL¿ n-Butyl Cyanoacrylate (n-BCA) Liquid Embolic System; Two 1 g tubes of n-BCA, one 10 mL vial of Ethiodized Oil and one 1 g vial of Tantalum Powder Product Code: 631-400; The TRUFILL n-BCA Liquid Embolic System is indicated for the embolization of cerebral arteriovenous malformations (AVMs) when pre-surgical devascularization is desired.
Reason for recall
Incorrect instructions for use (IFU).
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | Z-0788-2014 |
| Date reported | January 29, 2014 |
| Date initiated | October 11, 2013 |
| Recalling firm | Codman & Shurtleff, Inc. |
| Firm location | Raynham, MA |
| Affected scope | 3,860 |
| Distribution | Worldwide Distribution: US (nationwide) including Puerto Rico; and internationally to: Costa Rica and Russia. |
Profile values are sourced directly from the official FDA Devices 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 (Z-0788-2014) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. What to do next
This page summarizes the official FDA Devices 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? ▼
TRUFILL¿ n-Butyl Cyanoacrylate (n-BCA) Liquid Embolic System; Two 1 g tubes of n-BCA, one 10 mL vial of Ethiodized Oil and one 1 g vial of Tantalum Powder Product Code: 631-400; The TRUFILL n-BCA Liquid Embolic System is indicated for the embolization of cerebral arteriovenous malformations (AVMs) when pre-surgical devascularization is desired.. Recalled by Codman & Shurtleff, Inc.. Units affected: 3,860.
Why was this product recalled? ▼
Incorrect instructions for use (IFU).
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on January 29, 2014. Severity: Critical. Recall number: Z-0788-2014.
Where was the recalled product distributed? ▼
Distribution: Worldwide Distribution: US (nationwide) including Puerto Rico; and internationally to: Costa Rica and Russia..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0788-2014) against your product. Visit the official FDA Devices 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.
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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 Devices, reported January 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.