Arjo, Inc. Sling Rope/Connector Assembly Kits for the Sara and Sara Nova standing and raising aids; the kit is comprised of 2 x 200 cm ropes, 2 knobs, 2 sling connectors, 2 socket cap screws, 2 nylon nuts and 2 spacers; Arjo Inc., 50 N. Gary Avenue, Roselle, IL 60172; Model KS1006 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Sling Rope/Connector Assembly Kits for the Sara and Sara Nova standing and raising aids; the kit is comprised of 2 x 200 cm ropes, 2 knobs, 2 sling connectors, 2 socket cap screws, 2 nylon nuts and 2 spacers; Arjo Inc., 50 N. Gary Avenue, Roselle, IL 60172; Model KS1006
Brand
Arjo, Inc.
Lot Codes / Batch Numbers
Model KS1006, all kits shipped between July 2006 through September 2006
Products Sold
Model KS1006, all kits shipped between July 2006 through September 2006
Arjo, Inc. is recalling Sling Rope/Connector Assembly Kits for the Sara and Sara Nova standing and raising aids; the kit is due to The sling ropes were manufactured with insufficient rope length past the knot to prevent the knot from coming loose.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The sling ropes were manufactured with insufficient rope length past the knot to prevent the knot from coming loose.
Recommended Action
Per FDA guidance
Arjo Inc. USA sent recall letters to the direct accounts on 10/30/06, informing them that affected rope kits were incorrectly assembled, and could lead to the rope separating from the cone-shaped knob and causing the patient to fall back from the lift. The letters listed the specific quantities, order numbers and dates for the kits shipped to the customer, and requested the removal from use and return of the affected rope kits. Replacement rope kits were sent with the recall letters. Any questions were directed to Arjo''s Quality Department at 1-800-323-1245, ext. 6140.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026