BD (Becton, Dickinson and Company) (NYSE:BDX) has voluntarily executed a product recall of certain lots ofBD Q-Syte™ Luer Access Devices and BD Nexiva™ Closed IV Catheter Systems. Use of the affected devices may cause an air embolism or leakage of blood and/or therapy, which may result in serious injury or death.
Cousins Products, Llc, Issues An Allergy Alert On Undeclared Egg, Soy, And Wheat In Spinach Vinaigrette
Cousins Products, LLC, of Covington, LA is voluntarily recalling the following Spinach Vinaigrette in 16 oz. jars
Haifa Smoked Fish Inc. Issues An Allert On Uneviscerated Whole Schmaltz Herring
Haifa Smoked Fish, located in Queens, New York, is recalling Haifa brand vacuum packaged Whole Schmaltz Herring with the lot number 20, because the product was found to be uneviscerated.
Pierino Frozen Foods Inc. Issues an Allergy Alert on Undeclared Eggs in Its Jumbo Shells with Cheese
Pierino Frozen Foods Inc. of Lincoln Park, Michigan is recalling its 24 oz. packages of Pierino Frozen Foods’ “Jumbo Shells with Cheese” because they contain undeclared eggs. People who have an allergy or severe sensitivity to eggs run the risk of serious or life-threatening allergic reaction if they consume these products.
Global Commodities Inc. Issues Allergy Alert On Undeclared Sulfites In Aahu Barah Brand Dry Apricot
Global Commodities Inc. of Hicksville, NY is recalling its 0.50 lbs. packages of Aahu Barah brand Dry Apricot food treats because they contain undeclared Sulfites. People who have allergies to Sulfites run the risk of serious or life-threatening allergic reaction if they consume this product.
Edwards Lifesciences Aquarius Hemodialysis System: Recall
Information concerning the recall is currently unavailable. Please check back shortly.
Hettich Centrifuges with 2050 and 2076 Plastic Rotors: Recall
Plastic centrifuge rotor may crack, break apart and be forcefully ejected.
Infusion Set Needles [Manufactured by Nipro for Exelint]: Recall
Class I recall due to “coring” or dislodging of silicone cores or slivers from the ports into which they are inserted.
FDA Announces Class I Recall of Certain Infusion Set Needles
The U.S. Food and Drug Administration today announced a Class I recall of Exel/Exelint Huber needles, Exel/Exelint Huber Infusion Sets and Exel/Exelint “Securetouch+” Safety Huber Infusion Sets, manufactured by Nipro Medical Corporation for Exelint International Corporation.
Hettich Centrifuges Issues a North America and Canada Recall of Plastic Hematocrit Rotors
Hettich Centrifuges, Beverly, MA, is initiating a North America and Canada recall of
2050 and 2076 plastic hematocrit rotors that are used in combination with the Mikro 12-
24, Mikro 20, Haematokrit 20 and Haematokrit 24 bench top plastic centrifuges. These
plastic rotors have the potential to break apart resulting in pieces of the rotor to be
forcefully ejected through the plastic centrifuge housing.