FDA Device recall Z-1682-2017

Plum 360 Infusion Pump, Software Version 15.02

FDA Device
Class II
terminated
Published 2017-04-05

On 2017-04-05 the FDA classified a Class II recall of Plum 360 Infusion Pump, Software Version 15.02 by Hospira A Pfizer, citing depleted Battery alarm shows instead of Replace Battery. On battery power, ongoing therapy stops, alarms show and sound, pump shuts down after 3 minutes. On AC power, the pump reb….

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-1682-2017
Classification	Class II
Status	terminated
Initiated	2016-12-30
Published	2017-04-05
Last updated	2026-09-13 11:54 UTC
Company	Hospira A Pfizer
Distribution	US

Product

Plum 360 Infusion Pump, Software Version 15.02. The infusion pump is capable of delivering fluids for a variety of therapies such as parenteral, enteral, or epidural infusions

Reason

Depleted Battery alarm shows instead of Replace Battery. On battery power, ongoing therapy stops, alarms show and sound, pump shuts down after 3 minutes. On AC power, the pump reboots (takes about 25 seconds). Therapy can resume. AC power interruption of 3-7 seconds prompts an incorrect E323 alarm, ongoing therapy stop, and pump reboot. Longer power loss results in battery power operation.

Identifiers

code_info	List number 30010; all products with software version 15.02 distributed prior to January 16, 2017. Serial numbers 19… List number 30010; all products with software version 15.02 distributed prior to January 16, 2017. Serial numbers 19985403, 19985406, 19985408, 19985428, 19985439, 19985440, 19985450, 19985464, 19985878, 19985879, 19985880, 19985881, 19985882, 19985883, 19985884, 19985885, 19985886, 19985887, 19985889, 19985890, 19985891, 19985892, 19985893, 19985894, 19985895, 19985896, 19985897, 19985898, 19985899, 19985900, 19985901, 19985902, 19985903, 19985904, 19985905, 19985906, 19985907, 19985908, 19985909, 19985910, 19985911, 19985912, 19985913, 19985914, 19985915, 19985917, 19985918, 19985919, 19985920, 19985921, 19985922, 19985923, 19985924, 19985925, 19985926, 19985927, 19985928, 19985929, 19985930, 19985931, 19985933, 19985934, 19985935, 19985936, 19985937, 19985938, 19985939, 19985940, 19985942, 19985943, 19985944, 19985945, 19985946, 19985947, 19985948, 19985949, 19985950, 19985951, 19985952, 19985953, 19985954, 19985955, 19985956, 19985957, 19985958, 19985959, 19985960, 19985961, 199

code_info

List number 30010; all products with software version 15.02 distributed prior to January 16, 2017. Serial numbers 19…

List number 30010; all products with software version 15.02 distributed prior to January 16, 2017. Serial numbers 19985403, 19985406, 19985408, 19985428, 19985439, 19985440, 19985450, 19985464, 19985878, 19985879, 19985880, 19985881, 19985882, 19985883, 19985884, 19985885, 19985886, 19985887, 19985889, 19985890, 19985891, 19985892, 19985893, 19985894, 19985895, 19985896, 19985897, 19985898, 19985899, 19985900, 19985901, 19985902, 19985903, 19985904, 19985905, 19985906, 19985907, 19985908, 19985909, 19985910, 19985911, 19985912, 19985913, 19985914, 19985915, 19985917, 19985918, 19985919, 19985920, 19985921, 19985922, 19985923, 19985924, 19985925, 19985926, 19985927, 19985928, 19985929, 19985930, 19985931, 19985933, 19985934, 19985935, 19985936, 19985937, 19985938, 19985939, 19985940, 19985942, 19985943, 19985944, 19985945, 19985946, 19985947, 19985948, 19985949, 19985950, 19985951, 19985952, 19985953, 19985954, 19985955, 19985956, 19985957, 19985958, 19985959, 19985960, 19985961, 199

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-1682-2017%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.