Hospira, Inc. (NYSE: HSP), announced today it will initiate a voluntary nationwide recall to the user level for one lot of 0.25% Marcaine™ (Bupivacaine HCl Injection, USP), 10 mL, Single-dose Vial – Preservative Free (NDC 0409-1559-10), Lot 34-440-DD. The recall is due to a confirmed customer report of discolored solution with visible particles embedded in the glass as well as discolored solution.

Dominex Natural Foods, LLC, is voluntarily recalling its AngelBowls Corkscrew Pasta and Creamy Tomato Vodka Sauce with following day codes: 00914 and 01314; (“Corkscrew Pasta”) because its ingredients may include undeclared pine nuts, a potential allergen. The company has determined that a small number of cases were inadvertently mispackaged.

Wegmans Food Markets, Inc. has initiated a voluntary recall of all Wegmans Easter Bread (braided loaf) 17 oz., UPC 77890 32431 (all code dates) because it contains egg, which is not declared on the label. People who have an allergy or severe sensitivity to egg run the risk of serious or life-threatening allergic reaction if they consume this product.

Hickory Farms, Inc., the specialty food and holiday gift retailer today announced a voluntary recall of its Chipotle Ranch Sauce due to an undeclared allergen on its label. The Chipotle Ranch Sauce is formulated with buttermilk powder, a known allergen.

Hospira, Inc. (NYSE: HSP), announced today it will initiate a voluntary recall of one lot of 1% Lidocaine HCI Injection, USP to the user level due to a confirmed customer report of orange and black particulate within the solution and embedded within the glass vial.

Whole Foods Market Southwest Region is recalling mini butter croissants because they contain eggs, an undeclared allergen. 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.

(NASDAQ: CBST) today announced it is voluntarily recalling one lot of CUBICIN® (daptomycin for injection) to the user level due to the presence of particulate matter, reported via customer complaint and identified as glass particles, found in a single vial from this lot, produced by a contract manufacturer. The administration of glass particulate, if present in an intravenous drug, poses a potential safety risk to patients.

Hospira, Inc. (NYSE: HSP), announced today that on April 2, 2014, it informed customers of a nationwide recall of seven lots of Propofol Injectable Emulsion, USP, to the user level due to a glass defect located on the interior neck of the vial, which was identified during a retain sample inspection where the glass vial contained visible embedded metal particulate. Free-floating metal particulates were also identified in vials upon further analysis.

Nature’s Universe is voluntarily recalling all lots of old Thinogenics product (product sold prior to February 6, 2014, hereinafter the “Old Product”) to the user level after FDA analysis revealed that the Old Product contained undeclared sibutramine.