MAUDE Adverse Event Report: CARDINAL HEALTH CONTAINER SHARPS 5QT RED; CONTAINER, SHARPS

Model Number 8507SA

Device Problem Mechanical Problem (1384)

Patient Problem No Clinical Signs, Symptoms or Conditions (4582)

Event Type  malfunction  

Manufacturer Narrative

An investigation is currently underway.Upon completion, the results will be forwarded.

Event Description

The customer reported that the sharps containers are difficult to fill without the door sticking shut, issues with sharps getting stuck in door and staff almost having needle exposure.No patient injury reported.

Manufacturer Narrative

A lot number was not available for review; however, a lot will not be released without meeting all criteria.No samples or pictures have been provided.Without samples or pictures, we are unable to observe the reported condition.If samples or pictures are received, the complaint may be re-opened and the investigation continued.An exact root cause could not be determined as there was not enough information or evidence available.Based on the information available and the investigation findings, additional actions are deemed unnecessary at this time.If additional information is received warranting further analysis, the investigation will be resumed this complaint will be used for tracking purposes.

• Brand Name: CONTAINER SHARPS 5QT RED
• Type of Device: CONTAINER, SHARPS
• Manufacturer (Section D): CARDINAL HEALTH; 777 west street; mansfield MA 02048
• Manufacturer (Section G): CARDINAL HEALTH; 815 tek drive; crystal lake IL 60039 9002
• Manufacturer Contact: jill saraiva ; 777 west street; mansfield, MA 02048 ; 5086183640
• MDR Report Key: 15374214
• MDR Text Key: 305419415
• Report Number: 1424643-2022-00624
• Device Sequence Number: 1
• Product Code: MMK
• UDI-Device Identifier: 10884521023284
• UDI-Public: 10884521023284
• Combination Product (y/n): N
• Reporter Country Code: US
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: User Facility,Company Representative
• Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date: 10/05/2022

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Model Number: 8507SA
• Device Catalogue Number: 8507SA
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Initial Date Manufacturer Received: 08/25/2022
• Initial Date FDA Received: 09/07/2022
• Supplement Dates Manufacturer Received: 08/25/2022
• Supplement Dates FDA Received: 10/05/2022
• Type of Device Usage: A
• Patient Sequence Number: 1