-
BD Cathena Safety IV Catheter BD Multiguard Technology 18 GA x 1.25 IN recall
FDA
· Becton Dickinson Infusion Therapy Systems, Inc. · Class II
-
META-TAN LAG/COMPRESSION SCREW KIT 90MM/85MM recall
FDA
· Smith & Nephew, Inc. · Class II
-
Bard¿ Single Intragastric Linton Balloon Tube recall
FDA
· C.R. Bard Inc · Class I
-
Bard¿ Blakemore Esophageal-Nasogastric Tube (Intermediate) recall
FDA
· C.R. Bard Inc · Class I
-
Bard¿ Blakemore Esophageal-Nasogastric Tube (Child) recall
FDA
· C.R. Bard Inc · Class I
-
Bard Blakemore Esophageal-Nasogastric Tube (Adult) recall
FDA
· C.R. Bard Inc · Class I
-
Bard Minnesota Four Lumen Esophagogastric Tamponade Tube recall
FDA
· C.R. Bard Inc · Class I
-
Yellowstone Brown Sugar Molasses Baked Beans, NET WT… recall
FDA
· Vietti Acquisitions, LLC · Class I
-
MedicaLyte Liquid Bicarbonate Concentrate recall
FDA
· Nipro Renal Soultions USA, Corporation · Class I
-
Beijing Soybean Paste, packaged in 8.82 ounce/250g red and white packages recall
FDA
· May Flower International Inc · Class II
-
Philips Tempus Pro Patient Monitor recall
FDA
· Remote Diagnostic Technologies Ltd. · Class II
-
Item M7422, frozen foodservice Lamb Weston Hashbrown Patties LW Formed… recall
FDA
· LAMB WESTON Inc · Class II
-
Item M7414, frozen foodservice Lamb Weston Hashbrown Patties, frozen… recall
FDA
· LAMB WESTON Inc · Class II
-
Item M0053, frozen foodservice Lamb Weston Hashbrown Patties, frozen… recall
FDA
· LAMB WESTON Inc · Class II
-
Item M7204, frozen foodservice Lamb Weston Hashbrown Patties, frozen… recall
FDA
· LAMB WESTON Inc · Class II
-
Enhanced Verify Evaluation Handset (CFN HH90130FA) recall
FDA
· Medtronic Neuromodulation · Class II
-
Tibial Augment recall
FDA
· Waldemar Link GmbH & Co. KG (Mfg Site) · Class II
-
L-Shaped Femoral Augment recall
FDA
· Waldemar Link GmbH & Co. KG (Mfg Site) · Class II
-
Posterior Femoral Augment recall
FDA
· Waldemar Link GmbH & Co. KG (Mfg Site) · Class II
-
Distal Femoral Augment recall
FDA
· Waldemar Link GmbH & Co. KG (Mfg Site) · Class II
-
Quantum Informatics - VISION / LIVE VUE Product Name: Monitor… recall
FDA
· Spectrum Medical Ltd. · Class II
-
Quantum Informatics - VIPER Product Name: Monitor, Physiological… recall
FDA
· Spectrum Medical Ltd. · Class II
-
HistoCore PELORIS 3, Model recall
FDA
· Leica Biosystems Melbourne Pty Ltd · Class II
-
3.0 Liter Disposable Set (4 sets/case) recall
FDA
· Belmont Instrument LLC · Class II
-
Straight Inflow/Bifurcated Outflow Line Kit recall
FDA
· Belmont Instrument LLC · Class II
-
Straight Inflow/Outflow Patient Line Kit recall
FDA
· Belmont Instrument LLC · Class II
-
Hyperthermia Pump Procedure Kit recall
FDA
· Belmont Instrument LLC · Class II
-
Tempus Pro Patient Monitor, REFs: 00-1004-R (Tempus Pro non-printer, IBP… recall
FDA
· Remote Diagnostic Technologies Ltd. · Class II
-
Skytron Freedom 4FXS-60 Heavy Duty Monitor Mount recall
FDA
· Ihb Operations B.V. · Class II
-
Radiometer ABL90 Series - Radiometer ABL90 FLEX Model Number 393-090… recall
FDA
· Radiometer Medical ApS · Class II
-
CELL-DYN Ruby Product Name: CELL-DYN Ruby Model recall
FDA
· Abbott Laboratories · Class II
-
CELL-DYN Ruby Product Name: CELL-DYN Ruby Model recall
FDA
· Abbott Laboratories · Class II
-
CELL-DYN Ruby Product Name: CELL-DYN Ruby Model recall
FDA
· Abbott Laboratories · Class II
-
CELL-DYN Ruby Product Name: CELL-DYN Ruby Model recall
FDA
· Abbott Laboratories · Class II
-
CELL-DYN Ruby Product Name: CELL-DYN Ruby Model recall
FDA
· Abbott Laboratories · Class II
-
InPen smart insulin pen recall
FDA
· Medtronic MiniMed, Inc. · Class II
-
Merit Medical recall
FDA
· Merit Medical Systems, Inc. · Class II
-
Merit Medical recall
FDA
· Merit Medical Systems, Inc. · Class II
-
BD PYXIS MEDBANK (Name recall
FDA
· CareFusion 303, Inc. · Class II
-
NIM Vital Nerve Monitoring System: CONSOLE NIM4CM01 NIM 4.0 recall
FDA
· Medtronic Xomed, Inc. · Class II
-
Apple Juice recall
FDA
· S Martinelli & Company · Class II
-
Kapsin Ointment, Camphor 3.16% and Capsaicin 0.03%. Net Wt recall
FDA
· Apipharma · Class II
-
Hemopropin Ointment, Lanolin 17.76% and Petrolatum 71.2%, Net Wt recall
FDA
· Apipharma · Class II
-
Cerene Cryotherapy Device Product Name: DEVICE, THERMAL ABLATION… recall
FDA
· Channel Medsystems, Inc. · Class II
-
HeartMate Mobile Power Unit recall
FDA
· Thoratec LLC · Class I
-
MEDFLEX, REF: 1119-00; MEDBANK MAIN, REF: 1137-00; MEDFLEX 2.0… recall
FDA
· CareFusion 303, Inc. · Class II
-
Ballard Product Name: Closed Suction Catheters Model recall
FDA
· Avanos Medical, Inc. · Class I
-
Ballard Product Name: Closed Suction Catheters Model recall
FDA
· Avanos Medical, Inc. · Class I
-
Ballard Product Name: Closed Suction Catheters Model recall
FDA
· Avanos Medical, Inc. · Class I
-
Ballard Product Name: Closed Suction Catheters Model recall
FDA
· Avanos Medical, Inc. · Class I
-
Ballard Product Name: Closed Suction Catheters Model recall
FDA
· Avanos Medical, Inc. · Class I
-
Ballard Product Name: Closed Suction Catheters Model recall
FDA
· Avanos Medical, Inc. · Class I
-
Ballard Product Name: Closed Suction Catheters Model recall
FDA
· Avanos Medical, Inc. · Class I
-
Ballard Product Name: Closed Suction Catheters Model recall
FDA
· Avanos Medical, Inc. · Class I
-
Tandem Mobi Insulin Pump with Interoperable Technology recall
FDA
· Tandem Diabetes Care, Inc. · Class I
-
t:slim X2 Insulin Pump with Interoperable Technology recall
FDA
· Tandem Diabetes Care, Inc. · Class I
-
BD 4 Fr Single-Lumen PowerPICC Catheters recall
FDA
· Bard Access Systems, Inc. · Class I
-
BD Pyxis MedBank CUBIE Replenishment Station Product / Material ID BD… recall
FDA
· CareFusion 303, Inc. · Class II
-
BD Pyxis" MedBank" Mini and BD Pyxis" MedBank" Tower, BD Pyxis" MedFlex… recall
FDA
· CareFusion 303, Inc. · Class II
-
Hippo 072 Aspiration System including Cheetah Delivery Tool and Aspiration… recall
FDA
· Qapel Medical Inc. · Class I