Reported Nov 6, 2019 · Terminated
Kit, Port Access Product Code: DYNDC1582A
Centurion Medical Products Corporation
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: Centurion Medical Products Corporation · 100 Centurion Way · Williamston, MI · 48895-9086
Is this the product you have?
- Kit
- Port Access Product CodeDYNDC1582A
- Lot codes and dates
- Lot Number Expiration
20181213508/31/202020190207509/30/202020190315504/30/202120190415504/30/202120190617501/31/202120190624504/30/2021
- Lot Number Expiration
- Amount recalled
- 11260 kits
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
Why it was recalled
Supplier initiated recall of the GRIPPER Needles
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 Centurion Medical Products Corporation 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.