FDA recall record

Teleflex Medical Europe Baker Jejunostomy Tubes: Product Code Equivalent Code (a) 655300160 recall — FDA Z-1370-2018

These products contain latex, but the following statement is not included on any level of product packaging: Caution: This Product Contains Natural Rubber…

Class IIclassification
Z-1370-2018official record ID
Apr 18, 2018report date

Recall record at a glance

Official recordZ-1370-2018
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmTeleflex Medical Europe Ltd
Report dateApr 18, 2018
Recall initiation dateMar 15, 2018
Quantity200 units
LocationAthlone, Ireland

Official product description

Baker Jejunostomy Tubes: Product Code Equivalent Code (a) 655300160 655316 (b) 655500200 655520

Why the product 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.

Distribution information

US Nationwide Distribution

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Telephone.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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