RecallRadar

FDA Device recall Z-1620-2013

Bigliani/Flatow¿ The Complete Solution Fukuda Retractors Large Nonsterile 4305-19-40

On 2013-07-10 the FDA classified a Class II recall of Bigliani/Flatow¿ The Complete Solution Fukuda Retractors Large Nonsterile 4305-19-40 by Zimmer, citing this is a recall expansion from the 2010 recall which now includes seven additional lots that were not previously included. Zimmer, Inc. is initiating a recall of small and large….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1620-2013
ClassificationClass II
Statusterminated
Initiated2013-05-23
Published2013-07-10
Last updated2026-09-13 11:53 UTC
CompanyZimmer
DistributionUS

Product

Bigliani/Flatow¿ The Complete Solution Fukuda Retractors Large Nonsterile 4305-19-40. Used in retracting the humeral shaft posteriorly and exposing the entire glenoid surface.

Reason

This is a recall expansion from the 2010 recall which now includes seven additional lots that were not previously included. Zimmer, Inc. is initiating a recall of small and large Fukuda-type retractors due to fractures occurring at the grooves around the perimeter of the blades while being used during surgery.

Identifiers

code_info
Item Number: 00-4305-019-40 with Lot Numbers 61588143 and 61612276. 2010 Market Withdrawal: Item #:430501940 Lot #'s:…Item Number: 00-4305-019-40 with Lot Numbers 61588143 and 61612276. 2010 Market Withdrawal: Item #:430501940 Lot #'s: 60768814, 60806551, 60893241, 60946820, 60999665, 61031668, 61110808, 61170678, 61205673, 61244194, 61392456, 61430127

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1620-2013%22

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