FDA Recalls

FDA Drug Recall news

Philips Issues Worldwide Recall of Select Heartstart Fr2+ Automated External Defibrillators

Philips announced today that it is voluntarily recalling approximately 5,400 HeartStart FR2+ automated external defibrillators (AEDs). This recall is being conducted due to the possibility of a memory chip failure that may render the device inoperable.

Consumers Warned Not to Eat Certain Imported Dried Plums

The Texas Department of State Health Services is warning consumers not to eat certain imported dried plums and products containing imported dried plums because they have elevated levels of lead.

Neuron 6F 070 Delivery Catheter [Penumbra]

Field removal of the catheter due to reports that the catheter could kink or ovalize in certain anatomical situations, lead to difficulty in catheter advancement and/or delivery of other devices through the guide catheter

FDA Alert: New USP Standards for Heparin Products Will Result in Decreased Potency

The U.S. Food and Drug Administration today alerted health care professionals to a change in heparin manufacturing that is expected to decrease the potency of the common blood-clotting drug.

FDA Alert: New USP Standards for Heparin Products Will Result in Decreased Potency

The U.S. Food and Drug Administration today alerted health care professionals to a change in heparin manufacturing that is expected to decrease the potency of the common anti-clotting drug.

Penumbra Announces Worldwide Voluntary Field Removal of the Original Version of 6F Neuron 070 Delivery Catheter

Penumbra is initiating a voluntary Field Removal of the original version of Neuron 6F 070 Delivery Catheter. For these catheters, Penumbra has received feedback from some users that the catheter could kink or ovalize in certain anatomical situations.

Nationwide Voluntary Product Recall of Neocate® Infant Specialized Formula Lot P91877

Nutricia North America, Inc. (“Nutricia”) has contacted customers to undertake the voluntary recall and replacement of one (1) lot of the specialized infant formula product, Neocate®. This recall involves a limited quantity of individual cans (approximately 3700) from Lot # P91877, and does not affect any other Neocate® products or lot numbers.

Consumer Alert - Undeclared Sulfites in "Ziolopex Bakaliada Morele Suszone (Dried Apricots)"

New York State Agriculture Commissioner Patrick Hooker today alerted consumers that Adamba Imports International, Inc., located at 585 Meserole Street, Brooklyn, NY is recalling "Ziolopex Bakaliada Morele Suszone (Dried Apricots)” due to the presence of undeclared sulfites.

Price Rite 25 Ct Beef Bouillon is Being Voluntarily Recalled Due to Allergy Alert

Associated Brands Inc. of Medina, New York is voluntarily recalling 320 cases (3,840 selling units) of "Price Rite Beef Flavored Bouillon Cubes", lot code 22 JUL 11, as the lot has the potential to contain a dairy allergen which is not declared on the label. Consumers who have an allergy to milk may run the risk of a serious or life-threatening allergic reaction if they consume this product.

Americas Favorite Noshers Inc. Issues Alert on Unceclared Sulfites in Noshers Choice Brand Just Fruit

Americas Favorite Noshers Inc. of Brooklyn, New York 11205 is recalling Nosher's Choice brand Just Fruit because it contained undeclared sulfites. Consumers who have severe sensitivity to sulfites run the risk of serious or life-threatening allergic reactions if they consume this product.

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