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Terminated

G- Series Beds; G29 full length bed rails assembly

FDA Recall Z-1036-2015 · Posted 2015-02-02

Recalling FirmInvacare Corporation
Recall StatusTerminated
Product CodeFNL
Date Initiated2014-12-05
Date Terminated2015-06-18
Product Quantity2499 units

Reason for Recall

Invacare identified that the rail mounting bracket on the G29 full length bed rail was out of specification for entrapment safety.

Firm Action

Invacare sent an Urgent Medical Device Recall letter dated December 5, 2014, to all affected customers. The letter identified the product and the problem. Customers with questions should call 440-329-7996. For questions regarding this recall call 440-329-6875.

Root Cause

Nonconforming Material/Component

Distribution Pattern

US Nationwide Distribution including OH, CO, MO, and NY.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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