MAUDE Adverse Event Report: BD MEDICAL - DIABETES CARE WALGREENS THIN INSULIN SYRINGES 1.0ML 31GAUGE 5/16; PISTON SYRINGE

Catalog Number	928856
Medical Device Problem Code	Physical Resistance/Sticking (4012)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	08/10/2023
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that while using the walgreens thin insulin syringes 1.0ml 31gauge 5/16 there was difficulty aspirating.The following was received by the initial reporter: consumer reported finding when drawing inulin the plunger moves back to lower numbers on own.Plunger will not properly draw up insulin.Caller takes 30 units of insulin.Does not place air into the vial bottle.Was never informed to do so.
Additional Manufacturer Narrative
B.3.Date of event: unknown.The date received by manufacturer has been used for this field.H3.A device evaluation is anticipated but has not yet begun.Upon completion of the investigation, a supplemental report will be filed.
Additional Manufacturer Narrative
The following fields have been updated due to additional information: d.9.Device available for eval?: yes d.9.Returned to manufacturer on: 05oct2023.H.6.Investigation summary: samples were received and an investigation was performed.This is the 2nd complaint for the reported lot number.A review of the manufacturing records was performed and no non-conformances were raised in association with this type of event for this lot embecta was not able to duplicate or confirm the indicated issue and based on trend analysis no further action is required at this time.Complaints received for this device and reported condition will continue to be tracked and trended.
Event or Problem Description
It was reported that while using the walgreens thin insulin syringes 1.0ml 31gauge 5/16 there was difficulty aspirating.The following was received by the initial reporter: consumer reported finding when drawing inulin the plunger moves back to lower numbers on own.Plunger will not properly draw up insulin.Caller takes 30 units of insulin.Does not place air into the vial bottle.Was never informed to do so.

• Brand Name: WALGREENS THIN INSULIN SYRINGES 1.0ML 31GAUGE 5/16
• Common Device Name: PISTON SYRINGE
• Manufacturer (Section D): BD MEDICAL - DIABETES CARE; 1329 west highway 6; holdrege NE 68949
• Manufacturer (Section G): BD MEDICAL - DIABETES CARE; 1329 west highway 6; holdrege NE 68949
• Manufacturer Contact: jennifer suh ; 5859 farinon drive; san antonio, TX 78249 ; 8448235433
• MDR Report Key: 17634482
• Report Number: 1920898-2023-00584
• Device Sequence Number: 7749050
• Product Code: FMF
• UDI-Device Identifier: 00311917048130
• UDI-Public: (01)00311917048130
• Combination Product (Y/N): N
• Initial Reporter State: FL
• Initial Reporter Country: US
• PMA/510(K) Number: K024112
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Other,Consumer
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 11/02/2023

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
• Operator of Device: Lay User/Patient
• Device Catalogue Number: 928856
• Device Lot Number: 3030370
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 08/10/2023
• Supplement Date Received by Manufacturer: 11/02/2023
• Initial Report FDA Received Date: 08/28/2023
• Supplement Report FDA Received Date: 11/12/2023
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 01/30/2023
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Patient Sex: Unknown