Angio Pack #2 recall
ANGIO PACK #2; REF: DYNJ39185; Packaged in Mexico by: Medline Industries, Inc., Mundelein, IL 60060; 1-800-Medline; www.medline.com Surgical kit used to supply tools required to perform angiography medical procedures.
Why was Angio Pack #2 recalled?
Guidewire .035x150 3MMJ TCFC, item number 88241, has a potential for the coating to flake off of the wire. The guidewire is used in a number of surgical convenience kits assembled and marketed by Medline Industries, Inc.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Pack Number: DYNJ39185; Lots: 13EB2046, 13FB1553, 13GB2605
- Product
- ANGIO PACK #2; REF: DYNJ39185; Packaged in Mexico by: Medline Industries, Inc., Mundelein, IL 60060; 1-800-Medline; www.medline.com Surgical kit used to supply tools required to perform angiography medical procedures.
- Recalling firm
- Medline Industries, Inc.
- Quantity
- 768 units
- Distribution
- Nationwide Distribution: US to states of: AL, CA, FL, IL, LA, OH and VA.
- Recall date
- March 5, 2014
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (device)