[Recalled] CATH ANGIOGRAPHY DRAPE PACK; REF: DYNJ40851; Packaged in Mexico for Medline Industries, Inc., Mundelein, IL 60060; 1-800-Medline; www.medline.com Surgical kit used to supply tools required to perform medical procedures. — Guid
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | CATH ANGIOGRAPHY DRAPE PACK; REF: DYNJ40851; Packaged in Mexico for Medline Industries, Inc., Mundelein, IL 60060; 1-800-Medline; www.medline.com Surgical kit used to supply tools required to perform medical procedures. |
|---|---|
| Brand / manufacturer | Medline Industries, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1055-2014 |
| Country of notice | United States |
| Risk level | Class I |
| Hazard type | recall |
| Notice date | 14 August 2013 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: 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.
This Class I recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Stop using the product immediately and follow the authority's remedy (return, repair, or disposal).
Read the full official notice →
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This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.