Recall Register

Device recall: BD Syringe Tip Cap Bulk Sterile Convenience Pak-1000 units/shelf carton. Used to seal syringes and maintain container…

Class II FDA enforcement event 88805. Recall start date: . Status in the FDA record: Terminated. Termination date: .

Reason for recall, in the words of FDA

Holes in product packaging impacts package integrity and may compromise sterility.

Class II, in the words of FDA

a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote

Becton Dickinson & Company started this device recall on 27 Sep 2021. The firm address in the FDA record is in Franklin Lakes, NJ. FDA put the recall in Class II. FDA event 88805 has 1 product record. The first FDA enforcement report date is 3 Nov 2021. The record gives the status Terminated, with the termination date 4 May 2023.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Distribution

In the words of FDA.

TX

Recalling firm

Becton Dickinson & Company, Franklin Lakes, NJ.

Recalling firm: The firm that the FDA record names for a recall.

FDA records how the recall started: Voluntary: Firm initiated.

Products

1 product record in the event.

FDA event 88805: product records
Recall numberProductQuantityClassStatusReport date
Z-0179-2022BD Syringe Tip Cap Bulk Sterile Convenience Pak-1000 units/shelf carton. Used to seal syringes and maintain container closure integrity throughout the shelf life of the BD WWD syringe. Catalog Number: 3058228,000 unitsClass IITerminated3 Nov 2021

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Class II: The middle of the three FDA recall classes.

The event in context

Device events that started in 2021
900
Share of these events in Class II
89%
Product records in this event
1Median of the firm: 1
Events of the firm on the register
84

Other events of the firm

Other FDA enforcement events of Becton Dickinson & Company
InitiatedProduct (first record)TypeClassRecords
27 Apr 2026BD Spinal Tray with BD Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8DeviceClass I10
27 Jan 202610mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. 850 bulk non-sterile units per case.DeviceClass II1
14 Oct 2025BD Luer Tip Caps; Catalog Number(s) or Model Number(s): 308341;DeviceClass II1
16 Nov 2023PosiFlush Prefilled Saline Syringe with General Pump Compatibility (10mL Syringe with 10mL Saline Fill), Catalog Number DeviceClass II1
11 Oct 2023BD Alaris Pump infusion sets (Product Name, Catalog #) BD AlarisTM Pump Infusion Set Vented syringe adapter Smallbore TuDeviceClass II3
1 Feb 2023BD Ultra-Fine Insulin Syringe 0.5mL, 6mm, 31G - Insulin Syringes are designed for administering insulin in the treatmentDeviceClass II8
15 Sep 2022BD Vacutainer Tube Sodium Fluoride: 100 mg, Potassium Oxalate: 20 mg, Catalog Number 367001. For collecting, transportinDeviceClass II1
18 Jul 2022BD PhaSealTM Y-Site Connector (C80)- airtight and leak-proof Closed System Drug Transfer Device (CSTD) that mechanicallyDeviceClass II1
9 May 2022BD Connecta Stopcock with OFF Directed Tap Without Extension Tube (500 eaches/carton) Catalog No. 394910 (US)DeviceClass II11
6 Jan 2022BD Vacutainer Luer Lok Access Device - intended as a sterile, single use device designed to provide a connection to a caDeviceClass III1

Becton Dickinson & Company: all 84 events

Official channels

Cite this page

Recall Register. FDA enforcement event 88805. https://recallregister.com/fda/ii/88805/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA device enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
Newest FDA report date on the register
23 Sep 2026

FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.

Questions

Where was the product distributed?
The FDA record gives this distribution: TX
What quantity of product is in FDA event 88805?
The FDA record gives this quantity: 8,000 units
How did the recall start?
The FDA record says: Voluntary: Firm initiated
How many device recalls of 2021 have the same class?
89% of the 900 device events that started in 2021 are in Class II.