Z-0410-2014Class II

Vertebroplasty Needle Kit 10g Diamond Tip Intended to be used to inject PMMA cement into vertebral bodies...

Name: Z-0410-2014 Vertebroplasty Needle Kit 10g Diamond Tip Intended to be used to inject PMMA cement into vertebral bodies...
Creator: Synthes USA HQ, Inc.
Published: 2013-07-30
License: https://open.fda.gov/license/

Synthes GmbH / initiated 2013-07-30 / Terminated / root cause: packaging

FDA source

Synthes USA HQ, Inc. began a recall of Vertebroplasty Needle Kit 10g Diamond Tip Intended to be used to inject PMMA cement into vertebral bodies during Vertebroplasty procedure on 2013-07-30. FDA classified it as Class II and gives the reason as "Complaints were received of inconsistencies in the expiration dates shown on the packaging of the Vertebroplasty Needle Kit 10g Diamond Tip device". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as packaging.

Recall record

Recall number: Z-0410-2014
Classification: Class II
Status: Terminated
Initiated: 2013-07-30
Posted: 2013-11-27
Terminated: 2015-04-16
Recalling firm: Synthes GmbH
Product: Vertebroplasty Needle Kit 10g Diamond Tip Intended to be used to inject PMMA cement into vertebral bodies during Vertebroplasty procedure.
Product code: OAR Injector, Vertebroplasty (Does Not Contain Cement)
Reason for recall: Complaints were received of inconsistencies in the expiration dates shown on the packaging of the Vertebroplasty Needle Kit 10g Diamond Tip device.
Root cause tag: packaging
FDA root cause: Incorrect or no expiration date
Action: Synthes sent an Urgent Notice: Medical Device Notification letter dated October 8, 2013, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to returny any of the affect devices, call Synthes at 1-800-479-6329 to obtain a Return Authorization Number, complete the Verification Section indicating the affected product has been located, also indicate the number of devices found and note the Return Authorization Number. Return the Verification Form to: Credit/Returns Synthes 1101 Synthes Avenue Monument, CO 80132 Customers were also instructed to return the Verification Section even if they don't have the affected product. Customers with questions were instructed to call 610-719-5450 or contact their Synthes Sales Consultant. For questions regarding this recall call 610-719-5000.
Quantity in commerce: 40
Distribution: Nationwide Distribution including IN, MT, HI, and FL.
Product codes and lots: Part No. 03.702.218S, Lot No. AJM838X

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-0410-2014
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-0410-2014	Class II	Terminated	Voluntary: Firm initiated	2013-12-04	2013-11-26

Product code OAR

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)