Reported Jun 1, 2016 · Terminated
WHIN Infusion Set - 90 Huber Needle and Wing (22 ga/1in). Intravenous delivery through intravascular ports, 20 units…
B. Braun Medical, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: B. Braun Medical, Inc. · 901 Marcon Blvd · Allentown, PA · 18109-9512
Is this the product you have?
- WHIN Infusion Set - 90 Huber Needle and Wing (22 ga/1in). Intravenous delivery through intravascular ports, 20 units per case, Catalog Number 471734
- UsageInfusion of solution/medication into implanted intravascular ports
- Lot codes and dates
- Catalog Number 471734
- Lot Numbers0061482060 and 0061486821
- expiration dates1/31/2021 and 02/28/2021, respectively
- Amount recalled
- 5,980 units [Lot # 0061482060 (3,340 units); Lot # 0061486821 (2,640 units)]
Where it was sold
Why it was recalled
Potential for the tip of the Huber needle on the WHIN Infusion Set to protrude from the needle guard.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
Free recall alerts
Get alerted about new B. Braun Medical, Inc. recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.