LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter with introducer (eIFU) REF # e2400-53
Reported: March 22, 2017 Initiated: February 7, 2017 #Z-1445-2017
Product Description
LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter with introducer (eIFU) REF # e2400-53
Reason for Recall
The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
Details
- Recalling Firm
- LeMaitre Vascular, Inc.
- Units Affected
- 250
- Distribution
- Worldwide distribution. US Nationwide, AUSTRIA, BELGIUM, FRANCE, GERMANY, ITALY, LUXEMBOURG, Morocco, Saudi Arabia, Singapore, SPAIN, SWITZERLAND, UAE, and UK
- Location
- Burlington, MA
Frequently Asked Questions
What product was recalled? ▼
LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter with introducer (eIFU) REF # e2400-53. Recalled by LeMaitre Vascular, Inc.. Units affected: 250.
Why was this product recalled? ▼
The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 22, 2017. Severity: Moderate. Recall number: Z-1445-2017.
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