MAUDE Adverse Event Report: BECTON DICKINSON BD¿ SHARPS COLLECTOR; HYPODERMIC SINGLE LUMEN NEEDLE

Model Number	305609
Medical Device Problem Code	Component Missing (2306)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	04/20/2023
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Oem manufacturer: the manufacturing location for this product is flextronics.This site is an oem manufacturing site.Therefore, bd corporate headquarters in franklin lakes, nj has been listed and the franklin lakes fda registration number has been used for the manufacture report number.Date of event: unknown.The date received by manufacturer has been used for this field.A device evaluation is anticipated, but has not yet begun.Upon completion of the investigation, a supplemental report will be filed.
Event or Problem Description
It was reported that 5 boxes of bd¿ sharps collectors had no lids.The following information was provided by the initial reporter: "we have been stocking these 305609s and 305613s and we have problems with the lids.Our crews are having problems putting on the sliding lids.We have five (5) opens boxes of these sharps collectors with no lids.The five open cases of 305609s 19 gallon sharps collectors are of no use to us without lids.".
Event or Problem Description
It was reported that 5 boxes of bd¿ sharps collectors had no lids.The following information was provided by the initial reporter: "we have been stocking these 305609s and 305613s and we have problems with the lids.Our crews are having problems putting on the sliding lids.We have five (5) opens boxes of these sharps collectors with no lids.The five open cases of 305609s 19 gallon sharps collectors are of no use to us without lids.".
Additional Manufacturer Narrative
Investigation summary no product or photo was returned by the customer.It was reported by customer that "problems with the lids.Having problems putting on the sliding lids could not be verified due to the product not being returned for failure investigation.Dhr review process to verify if there were issues reported as missing lids or lid will not shut issue during the manufacturing process of this product was not able to be performed since no lot number was provided.A review of ncmr¿s was performed; the results exhibit no issues reported for the same part number and issues throughout the last twelve months.
Event or Problem Description
It was reported that the bd¿ sharps collectors lids were not closing properly.The following information was provided by the initial reporter: verbatim "we have been stocking these 305609s and 305613s and we have problems with the lids.Our crews are having problems putting on the sliding lids.We have five (5) opens boxes of these sharps collectors with no lids.The five open cases of (b)(4) 19 gallon sharps collectors are of no use to us without lids." per phone call we spoke to the customer over the phone today and this was his response, "there is a grey seal and they're not fitting on the containers right.The team could not get the product to seal.The customer threw the lids away if they didn't work.The customer was not missing lids, but since they were being discarded, the stock was low.
Additional Manufacturer Narrative
Correction: b5: describe event or problem: it was reported that the bd¿ sharps collectors lids were not closing properly.The following information was provided by the initial reporter: verbatim."we have been stocking these 305609s and 305613s and we have problems with the lids.Our crews are having problems putting on the sliding lids.We have five (5) opens boxes of these sharps collectors with no lids.The five open cases of 305609s 19 gallon sharps collectors are of no use to us without lids."" per phone call we spoke to the customer over the phone today and this was his response, "there is a grey seal and they're not fitting on the containers right.The team could not get the product to seal.The customer threw the lids away if they didn't work.The customer was not missing lids, but since they were being discarded, the stock was low.

• Brand Name: BD¿ SHARPS COLLECTOR
• Common Device Name: HYPODERMIC SINGLE LUMEN NEEDLE
• Manufacturer (Section D): BECTON DICKINSON; 1 becton drive; franklin lakes NJ 07417
• Manufacturer (Section G): BECTON DICKINSON; 1 becton drive; franklin lakes NJ 07417
• Manufacturer Contact: phillip emmert ; 9450 south state street; sandy, UT 84070 ; 8448235433
• MDR Report Key: 16920391
• Report Number: 2243072-2023-00785
• Device Sequence Number: 6720184
• Product Code: FMI
• UDI-Device Identifier: 00382903056095
• UDI-Public: 00382903056095
• Combination Product (Y/N): N
• Initial Reporter State: CO
• Initial Reporter Country: US
• PMA/510(K) Number: K943575
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Other,User Facility
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 06/27/2023

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: Other
• Device Model Number: 305609
• Device Catalogue Number: 305609
• Device Lot Number: UNKNOWN
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 04/20/2023
• Supplement Date Received by Manufacturer: 06/09/2023; 06/27/2023
• Initial Report FDA Received Date: 05/12/2023
• Supplement Report FDA Received Date: 06/23/2023; 07/13/2023
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• 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