MAUDE Adverse Event Report: MEDLINE INDUSTRIES, LP MEDLINE; SLING,MESH,FULL BODY,COMMODE,XL

Catalog Number	MDSMR116
Medical Device Problem Codes	Break (1069); Material Integrity Problem (2978)
Health Effect - Clinical Code	Fall (1848)
Date of Event	04/20/2026
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
According to the facility, "we had a resident being transferred with a total lift sling.The resident weighs 275# both lower leg loops broke during transfer dropping the resident.The resident is now in the er.The sling showed no signs of fraying, thinning, or concerns over its integrity." no additional information at this time.Due diligence has been completed.No additional details are available related to the customer reported issue.It has been determined that the reported event could cause or contribute to serious injury if it were to occur.In an abundance of caution, this medwatch is being filed.If any further relevant information is identified or obtained, a supplemental medwatch will be submitted.
Event or Problem Description
According to the facility, "we had a resident being transferred with a total lift sling.The resident weighs 275# both lower leg loops broke during transfer dropping the resident.

• Brand Name: MEDLINE
• Common Device Name: SLING,MESH,FULL BODY,COMMODE,XL
• Manufacturer (Section D): MEDLINE INDUSTRIES, LP; three lakes drive; northfield IL 60093 2753
• Manufacturer Contact: alyssa reasner ; three lakes drive; northfield, IL 60093-2753
• MDR Report Key: 25164257
• Report Number: 1417592-2026-01270
• Device Sequence Number: 15997923
• Product Code: FSA
• UDI-Device Identifier: 10884389128770
• UDI-Public: 10884389128770
• Combination Product (Y/N): N
• Initial Reporter State: OK
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 05/13/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Device Catalogue Number: MDSMR116
• Was Device Available for Evaluation?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 04/20/2026
• Initial Report FDA Received Date: 05/13/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Unknown
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Age: 87 YR
• Patient Sex: Female
• Patient Weight: 125 KG