55715 articles — Page 156 of 2786
FDA recall notice for "Tacos de Camarones" (Shrimp-filled turnovers)***Keep Refrigerated***Manufacturado por Sun Boricua Pa'l Mundo Inc, Carr. 486 km 0.1 Bo. Qu
FDA recall notice for "Tacos de Langosta" (Lobster-filled turnovers)***Keep Refrigerated***Manufacturado por Sun Boricua Pa'l Mundo Inc, Carr. 486 km 0.1 Bo. Qu
FDA recall notice for "Tacos de Jueyes" (Crabmeat-filled turnovers)***Keep Refrigerated***Manufacturado por Sun Boricua Pa'l Mundo Inc, Carr. 486 km 0.1 Bo. Que
FDA recall notice for Queso Pringles, 40 g , and Cont. Neto Net Weight: 139 g( 4.9 oz) Queso /Cheese; Busting with more Flavor "Ahora con Man Sabor" (Kellogg
FDA recall notice for "Tacos de Marlin" (Marlin-filled turnovers)***Keep Refrigerated***Manufacturado por Sun Boricua Pa'l Mundo Inc, Carr. 486 km 0.1 Bo. Quebr
FDA recall notice for Korean Molluscan Shellfish (Seasoned Oysters) 250kg, 1000kg (Hamchorom Inc.). Reason: The recall was initiated because Hamchorom dba Golde
FDA recall notice for Large IQF Oysters, 6 x 4 lb/cs (Ocean Group Inc.). Reason: Ocean Group is recalling tiny IQF oysters, large IQF oysters, and half shelf oy
FDA recall notice for half shell Oysters, 144pc/cs (Ocean Group Inc.). Reason: Ocean Group is recalling tiny IQF oysters, large IQF oysters, and half shell oy
FDA recall notice for Tiny IQF Oysters, 40pk/cs, 8oz. (Ocean Group Inc.). Reason: Ocean Group is recalling tiny IQF oysters, large IQF oysters, and half shell o
FDA recall notice for Sysmex XE-5000 Automated Hematology System; an automated differential cell counter; Sysmex Corporation, Kobe, Japan; Sysmex America, One
FDA recall notice for I-Flow ON-Q Pain Relief System, T-Block Needle/Catheter Kit, Model #TB089T The intended use of each component in the finished final tra
FDA recall notice for I-Flow ON-Q Pain Relief System, T-Block Needle/Catheter Tray, Model #TBTB1089T The intended use of each component in the finished final
FDA recall notice for Bayonet Forceps 7.-1/8 (181.0mm) 0.75mm Insulated Tips, Sterile Single Use Surgical/Bipolar Forceps, Model #20-1360I, 510 (k) #K884656. T
FDA recall notice for Bayonet Forceps 8.5" (215.9mm) Serrated 1.0 mm Tips Electrosurgical/Monopolar Forceps/Reusable, Model #41604, 510 (k) #K885199. The surgic
FDA recall notice for Irrigating Bayonet Forceps 8.25" (209.6 mm) 1.5 mm Tips, Electrosurgical Irrigating Bipolar Forceps, Model #20-0431, 510 (k) #K072937. Eac
FDA recall notice for CIDEX OPA, High Level Disinfectant Solution, Glutaraldehyde-free (0.55% ortho-phthaladehyde) solution. The CIDEX OPA solution is intended
FDA recall notice for Bayonet Forceps 7.75" (196.9 mm) 0.5 mm Tips Non-Stick Electrosurgical/Bipolar Forceps/Reusable, Model #90-7004 (k) #K982705. The surgic
FDA recall notice for Bayonet Forceps 7.-1/8 (181.0mm) 0.75mm Non-Insulated Tips, Sterile Single Use Surgical/Bipolar Forceps, Model #20-1360K 510 (k) #K884656.
FDA recall notice for T5 Hytrel Zipper Toga. Product Usage: The togas are intended to provide a barrier between the operating room and the members of the s
FDA recall notice for Sysmex XE-2100C Automated Hematology System; an automated differential cell counter; Sysmex Corporation, Kobe, Japan; Sysmex America, One