ALWAYS *

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2004-01-29 for ALWAYS * manufactured by *.

Event Text Entries

[335889] The complainant purchased a 24 package of always maxi-pads at none grocery store. They used approx 10 pads and when going to get another pad from the plastic container; they saw a syringe/needle inside the package. The complainant contacted the sheriff's department and spoke with deputy. Deputy collected the needle, the packaging, and the receipt for the purchase.
Patient Sequence No: 1, Text Type: D, B5

MAUDE Entry Details

• Report Number: MW4003712
• MDR Report Key: 526515
• Date Received: 2004-04-28
• Date of Report: 2004-01-29
• Date Added to Maude: 2004-05-26
• Event Key: 0
• Report Source Code: Voluntary report
• Manufacturer Link: N
• Number of Patients in Event: 0
• Adverse Event Flag: 3
• Product Problem Flag: 3
• Reprocessed and Reused Flag: 3
• Reporter Occupation: PATIENT
• Health Professional: 3
• Initial Report to FDA: 0
• Report to FDA: 0
• Event Location: 3
• Single Use: 0
• Previous Use Code: 0
• Event Type: 3
• Type of Report: 3

Device Details

• Brand Name: ALWAYS
• Generic Name: MAXI-PADS
• Product Code: HHL
• Date Received: 2004-01-29
• Model Number: *
• Catalog Number: *
• Lot Number: *
• ID Number: *
• Device Availability: *
• Implant Flag: N
• Date Removed: *
• Device Sequence No: 1
• Device Event Key: 515685
• Manufacturer: *
• Manufacturer Address: * * US

Patients

Patient Number	Treatment	Outcome	Date
1	0		2004-04-28