Reported Apr 18, 2018 · Terminated
Baker Jejunostomy Tubes: Product Code Equivalent Code (a) 655300160 655316 (b) 655500200 655520
Teleflex Medical Europe Ltd.
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: Teleflex Medical Europe Ltd · Ida Business Park · Athlone · N/A
Is this the product you have?
- Baker Jejunostomy TubesProduct Code Equivalent Code (a) 655300160 655316 (b) 655500200 655520
- Lot codes and dates
- (a) 655300160 655316 Batch Numbers 13EG28 13HG23 (b) 655500200 655520
- Batch Numbers13EG28
- Amount recalled
- 200 units
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
- Nationwide
Why it was recalled
These products contain latex, but the following statement is not included on any level of product packaging: Caution: This Product Contains Natural Rubber Latex Which May Cause Allergic Reactions.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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