Reported Apr 24, 2013 · Terminated

OsteoSelect DBM Putty Product Usage: Orthopedic bone filler

Bacterin International, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Bacterin International, Inc. · 600 Cruiser Ln · Belgrade, MT · 59714-9719

Is this the product you have?

  • OsteoSelect DBM Putty Product UsageOrthopedic bone filler
Lot codes and dates
  • B100164 and B110115
Amount recalled
165

Where it was sold

  • Nationwide

Why it was recalled

The firm's retesting procedure was not validated.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Bacterin International, Inc. recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Jul 1, 2013 · Data as of Sep 19, 7:25 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.