RecallRadar

FDA Device recall Z-2353-2016

S3 MedSurg Bed, Model 3005

On 2016-08-17 the FDA classified a Class II recall of S3 MedSurg Bed, Model 3005 by Stryker Medical Division, citing CPU board failures cause fowler (backrest) electronic controls to stop working.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2353-2016
ClassificationClass II
Statusterminated
Initiated2016-02-02
Published2016-08-17
Last updated2026-09-13 11:54 UTC
CompanyStryker Medical Division
DistributionUS

Product

S3 MedSurg Bed, Model 3005. Stryker Medical

Reason

CPU board failures cause fowler (backrest) electronic controls to stop working.

Identifiers

code_info
MDL#: E341062; 3005S3EX; 3005S3Patriot; 3005S3Signature; 3005S3PX1; 3005S3PX2; 3005S3PX3; 3005S3PX4; 3005S3EX; Serial N…MDL#: E341062; 3005S3EX; 3005S3Patriot; 3005S3Signature; 3005S3PX1; 3005S3PX2; 3005S3PX3; 3005S3PX4; 3005S3EX; Serial Numbers: 141115067 through 150615027; Serial Numbers: 141115067 141115068 141115069 141115070 141115071 141115072 141115073 141115074 141115075 141115076 141115077 141115078 141115079 141115080 141115081 141115082 141115083 141115084 141115085 141115086 141115087 141115088 141115089 141115090 141115091 141115092 141115093 141115094 141115095 141115096 141115097

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2353-2016%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.