RecallDepth

Bed Assist Bars, labeled as follows: a) Medline, Model Number BA6800, b) Medline Martha Stewart, Model Number MDS6800BAMMS

This recall is currently active, issued April 5, 2024. It was issued by Medline Industries, Lp - Northfield.

Company
Medline Industries, Lp - Northfield
Recall Initiated
March 5, 2024
Posted
April 5, 2024
Recall Number
Z-1487-2024
Quantity
2895 devices
Firm Location
Northfield, IL
Official Source
View on FDA website ↗

Reason for Recall

Medline is recalling certain lots of our Adult Portable Bed Rails that were manufactured after the mandatory compliance requirement (ASTM F3186-17, Standard Specification for Adult Portable Bed Rails and Related Products and 16 CFR Part 1270, Safety Standard for Adult Portable Bed Rails) and failed to meet all mandatory requirements outlined in these standards.

Distribution

Worldwide distribution - US Nationwide and the country of Canada.

Lot / Code Info

a) Medline, Model Number BA6800, Lot Numbers: 88523090002, 88523090003, 88523100001, 88523100002, 88523100003, 88523110002, 88523110003, 88523120002, 88523120003, 88524010002, 88524020001, 88524020002, 88524030001; b) Medline Martha Stewart, Model Number MDS6800BAMMS, Lot Numbers: 39323090001, 39323090002, 39323100001, 39323100002, 39323110001, 39323110002, 39323120001, 39323120002, 39324010001, 39324010002;

Root Cause

Under Investigation by firm

Action Taken

Medline Industries, LP issued a Medical Device Recall Notice to its consignees on 03/05/2024 via USPS first class mail and email. The notice explained the issue with the device and requested the consignee destroy the device. Distributors were directed to notify their customers.

More recalls by Medline Industries, Lp - Northfield

View all recalls by this company →