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Baxter Healthcare Corp. recalls Baxter Non-DEHP Micro-Volume Extension Set, Male Luer Lock Adapter, 36 (91 cm), Volume 0.32 mL; an Rx sterile, single us
Recalled September 7, 2016 · FDA recall Z-2687-2016 · Baxter Healthcare
Hazard
Some of the individual extension set packages were improperly sealed, compromising the sterility of the product. · FDA Class II
Units
15,257 units
Sold at
Worldwide Distribution - US including FL, GA, IL, KS, KY, MI, MO, NC, ND, OH, PA, SC, TN, TX, WV, Puerto Rico and Internationally to Canada.
Description
Some of the individual extension set packages were improperly sealed, compromising the sterility of the product.
Product
Baxter Non-DEHP Micro-Volume Extension Set, Male Luer Lock Adapter, 36 (91 cm), Volume 0.32 mL; an Rx sterile, single use nonpyrogenic fluid pathway; 50 sets per case; For the administration of drugs and solutions to a patient's vascular system through a vascular access device.
Manufacturer(s)
Baxter Healthcare Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →