-
CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented… recall
FDA
· Baxter Healthcare Corporation · Class II
-
CLEARLINK System Non_DEHP Extenstion Set, Straight-Type Extension Set… recall
FDA
· Baxter Healthcare Corporation · Class II
-
CLEARLINK SYSTEM EXTENSION SET, Straight-Type Extension Set… recall
FDA
· Baxter Healthcare Corporation · Class II
-
CLEARLINK SYSTEM EXTENSION SET, Straight-Type Extension Set… recall
FDA
· Baxter Healthcare Corporation · Class II
-
CLEARLINK SYSTEM EXTENSION SET, Straight-Type Extension Set… recall
FDA
· Baxter Healthcare Corporation · Class II
-
CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, 0.2 Micron Filter… recall
FDA
· Baxter Healthcare Corporation · Class II
-
CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, 0.2 Micron Filter… recall
FDA
· Baxter Healthcare Corporation · Class II
-
CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented… recall
FDA
· Baxter Healthcare Corporation · Class II
-
CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented… recall
FDA
· Baxter Healthcare Corporation · Class II
-
CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented… recall
FDA
· Baxter Healthcare Corporation · Class II
-
CLEARLINK SYSTEM Solution Set, Non-Vented, two CLEARLINK Luer Activated… recall
FDA
· Baxter Healthcare Corporation · Class II
-
CLEARLINK System Solution Set, DUO-VENT, CLEARLINK Luer Activated Valve… recall
FDA
· Baxter Healthcare Corporation · Class II
-
CONTINU-FLO Solution Set, Non-Vented, two CLEARLINK Luer Activated Valves… recall
FDA
· Baxter Healthcare Corporation · Class II
-
Branding is not applied to this product recall
FDA
· Spacelabs Healthcare, Inc. · Class II
-
Branding is not applied to this product recall
FDA
· Spacelabs Healthcare, Inc. · Class II
-
Branding is not applied to this product recall
FDA
· Spacelabs Healthcare, Inc. · Class II
-
DuoDERM" Extra Thin dressings are highly flexible… recall
FDA
· ConvaTec, Inc · Class II
-
Airvo 2, REF: PT101US, and myAirvo 2, REF: PT100US… recall
FDA
· Fisher & Paykel Healthcare, Ltd. · Class II
-
BioPro Femoral Head Product ID/Description 14089 HEAD FEMORAL 28 SH LT… recall
FDA
· BioPro, Inc. · Class II
-
BioPro Endo Head (Ceramic) Product ID/Description 13006 ENDO MODULAR… recall
FDA
· BioPro, Inc. · Class II
-
BioPro Femoral Head (Ceramic heads 28-30) Product ID/Description 19023… recall
FDA
· BioPro, Inc. · Class II
-
BioPro Bipolar Head Product ID/Description 18130 BIPOLAR HEAD 38MM 18131… recall
FDA
· BioPro, Inc. · Class II
-
BioPro Endo Head (Metal uni-polar, 38-55) Product Number/Description 10179… recall
FDA
· BioPro, Inc. · Class II
-
BioPro Femoral Head (Metal 22, 28, 32, 36, 40) cobalt chromium and ceramic… recall
FDA
· BioPro, Inc. · Class II
-
ARVIS Product Name: ARVIS" Shoulder Model recall
FDA
· Kico Knee Innovation Company · Class II
-
C-Rex UNO Microinterventional Goniotomy Instrument recall
FDA
· Iantrek Inc. · Class II
-
Cyclopen Microinterventional Cyclodialysis System recall
FDA
· Iantrek Inc. · Class II
-
Zenith Alpha 2 Thoracic Endovascular Graft recall
FDA
· Cook Medical Incorporated · Class I
-
6+ Months SPROUT ORGANICS Made With Organic Sweet Potato… recall
FDA
· Sprout Organics Inc. · Class II
-
Gluten Free Bean & Rice Burrito recall
FDA
· Amy's Kitchen Inc. · Class II
-
Design Options, PERIFIX FX Epidural Anesthesia Tray recall
FDA
· B Braun Medical Inc · Class II
-
Combined Spinal and Epidural Anesthesia Tray 2, PERIFIX 17 Ga recall
FDA
· B Braun Medical Inc · Class II
-
Design Options, Pain Management Tray recall
FDA
· B Braun Medical Inc · Class II
-
Combined Spinal and Epidural Anesthesia Tray, PERIFIX 17 Ga recall
FDA
· B Braun Medical Inc · Class II
-
ESPOCAN Combined Spinal and Epidural Anesthesia Tray, ESPOCAN 17 Ga recall
FDA
· B Braun Medical Inc · Class II
-
PERIFIX FX Continuous Epidural Anesthesia Set… recall
FDA
· B Braun Medical Inc · Class II
-
PERIFIX FX Continuous Epidural Anesthesia Tray, PERIFIX 17 Ga recall
FDA
· B Braun Medical Inc · Class II
-
PERIFIX FX Continuous Epidural Anesthesia Tray, PERIFIX 17 Ga recall
FDA
· B Braun Medical Inc · Class II
-
PERIFIX FX Continuous Epidural Anesthesia Tray, 17 Ga recall
FDA
· B Braun Medical Inc · Class II
-
PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga recall
FDA
· B Braun Medical Inc · Class II
-
PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga recall
FDA
· B Braun Medical Inc · Class II
-
PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga recall
FDA
· B Braun Medical Inc · Class II
-
PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga recall
FDA
· B Braun Medical Inc · Class II
-
EverPatch+ recall
FDA
· Corneat Vision, Ltd. · Class II
-
CorNeat EverPatch recall
FDA
· Corneat Vision, Ltd. · Class II
-
Organic BABY bedtime drops recall
FDA
· M.O.M Enterprises, LLC. · Class II
-
Kirkland Signature brand Ahi Tuna Wasabi Poke, Costco #17193, net wt recall
FDA
· Western United Fish Company Inc · Class I
-
Venclose digiRF Generators, Model VCRFG1, with software 3.35 designed to… recall
FDA
· Bard Peripheral Vascular Inc · Class II
-
JUNCTIONAL EMERGENCY TREATMENT TOOL (JETT) recall
FDA
· North American Rescue LLC. · Class II
-
GORE ACUSEAL Vascular Graft recall
FDA
· W L Gore & Associates, Inc. · Class II
-
NES Reprocessed 2.0mm RX Turbo Elite Laser Atherectomy Catheter recall
FDA
· Northeast Scientific Inc. · Class II
-
NES Reprocessed 1.7mm RX Turbo Elite Laser Atherectomy Catheter recall
FDA
· Northeast Scientific Inc. · Class II
-
NES Reprocessed 1.4mm RX Turbo Elite Laser Atherectomy Catheter recall
FDA
· Northeast Scientific Inc. · Class II
-
NES Reprocessed 0.9mm RX Turbo Elite Laser Atherectomy Catheter recall
FDA
· Northeast Scientific Inc. · Class II
-
NES Reprocessed 2.0mm OTW Turbo Elite Laser Atherectomy Catheter recall
FDA
· Northeast Scientific Inc. · Class II
-
NES Reprocessed 1.7mm OTW Turbo Elite Laser Atherectomy Catheter recall
FDA
· Northeast Scientific Inc. · Class II
-
NES Reprocessed 1.4mm OTW Turbo Elite Laser Atherectomy Catheter recall
FDA
· Northeast Scientific Inc. · Class II
-
NES Reprocessed 0.9mm OTW Turbo Elite Laser Atherectomy Catheter recall
FDA
· Northeast Scientific Inc. · Class II
-
IMPLANT EPIKUT PLUS MT16 3,5X10,0MM recall
FDA
· S.I.N. Implant System Ltda · Class II
-
16/25 Frozen Cooked Tail-On Farm Raised Shrimp recall
FDA
· Lawrence Wholesale LLC · Class II