FDA Device recall Z-1285-2015

GE Healthcare, Treadmill T2100 and Treadmill T2000 with power cord part numbers 408930-001 Rev E, 408930-002 Rev C, or 2028038-008 Rev B. A…

FDA Device
Class II
terminated
Published 2015-03-25

On 2015-03-25 the FDA classified a Class II recall of GE Healthcare, Treadmill T2100 and Treadmill T2000 with power cord part numbers 408930-001 Rev E, 408930-002 Rev C, or 2028038-008 Rev B. A… by Ge Healthcare, citing potential safety issue due to improper assembly associated with the power cords of T2100 and T2000 Treadmills.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-1285-2015
Classification	Class II
Status	terminated
Initiated	2015-02-16
Published	2015-03-25
Last updated	2026-09-13 11:53 UTC
Company	Ge Healthcare
Distribution	DC, PR

Product

GE Healthcare, Treadmill T2100 and Treadmill T2000 with power cord part numbers 408930-001 Rev E, 408930-002 Rev C, or 2028038-008 Rev B. Also Field Replaceable Unit P/Ns 408930-001 Rev E, 408930-002 Rev C. UPDATE: 3-30-2015: T2100 & T2000 Treadmills with power cord part numbers 408930-001, 408930-002, or 2028038-008 Also Field Replaceable Unit P/Ns 408930-001, 408930-002 Product Usage: Used for Exercise Testing, facilitating accurate blood pressure measurements and exercise testing within speed range of 0-13.5 miles per hour.

Reason

Potential safety issue due to improper assembly associated with the power cords of T2100 and T2000 Treadmills.

Identifiers

code_info	Mfg Lot or Serial # 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 40… Mfg Lot or Serial # 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-002 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-

code_info

Mfg Lot or Serial # 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 40…

Mfg Lot or Serial # 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-002 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-001 408930-

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-1285-2015%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.