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Letters |15 February 1997

Midline Catheters: The Final Chapter

Leonard Mermel, DO, ScM

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  • Rhode Island Hospital, Providence, RI 02903
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TO THE EDITOR:
On 18 September 1996, Johnson & Johnson Medical, Inc., withdrew the Streamline peripheral catheter, Landmark midline catheter, and Centermark peripherally inserted central catheter from the U.S. market. All of these intravascular catheters are made of the unique copolymer Aquavene. This event reflects the culmination of investigations by the Food and Drug Administration (FDA) [1] and others [2, 3], which showed that these catheters, unlike any others on the U.S. market, are associated with life-threatening anaphylactoid reactions. Important lessons are to be learned, as eloquently expressed in the editorial [4] that accompanied our report [2]. Namely,...
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Mermel L. Midline Catheters: The Final Chapter. Ann Intern Med. 1997;126:334. doi: https://doi.org/10.7326/0003-4819-126-4-199702150-00026

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Published: Ann Intern Med. 1997;126(4):334.

DOI: 10.7326/0003-4819-126-4-199702150-00026

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