Reported Feb 14, 2018 · Terminated
Lumbar Puncture Tray, Catalog # 1862 Product Usage: Surgical procedure
Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables
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: Robert Busse & Co. Inc. d.b.a. Busse Hospital Disposables · 75 Arkay Dr · Hauppauge, NY · 11788-3707
Is this the product you have?
- Lumbar Puncture Tray, Catalog # 1862
- Product UsageSurgical procedure
- Lot codes and dates
7 of 7 products
Products covered by this recall # Product as published 1 1710206/Expiration Date: 05/30/2022 2 1710040/Expiration Date: 01/30/2022 3 1610536/Expiration Date: 12/30/2021 4 1610423/No Expiration Date 5 1610351/No Expiration Date 6 1610219/No Expiration Date 7 1610090/No Expiration Date - Amount recalled
- 1037 in total
This recall covers 7 products
The agency filed one notice per product. You are reading one of them; the other 6 are below.
Where it was sold
- Nationwide
Why it was recalled
BD SafetyGlide Needle 22GA 1-1/2 inch may contain the presence of loose polyprophylene foreign matter above release specification.
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 foreign material 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.