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Recall archive

94,355 stored notices, from Jun 20, 2012 to Sep 23, 2026.

26 recalls · page 2 of 2

Medical devices

Reported Aug 22, 2012

Synthes(R) Hemostatic Bone Putty, Part numbers 08.901.001.97S, 08.901.001.98S, 08.901.001.99S, 08.901.001D, and…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Synthes USA HQ, Inc.

Matched: Brand · Product · Product details — There is the potential for Hemostatic Bone Putty to ignite if contacted with electrosurgical cautery systems under certain conditions during surgery.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2012

4.5mm TI Multiloc Screw Length 38MM-Sterile Expiration: 04/29/2012 REF 04.019.038S Manufactured or Distributed by…

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

Synthes USA HQ, Inc.

Matched: Brand · Product details — Two lots of 4.5mm multi-loc screws were recalled due to incorrect labeling of screw size.

1 more product in this recall

FDA (openFDA device enforcement)

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