-
BECKMAN COULTER BICARBONATE recall
FDA
· Beckman Coulter Ireland, Inc. · Class II
-
da Vinci 5, Surgeon Console Column Motor Connector recall
FDA
· Intuitive Surgical, Inc. · Class II
-
BD Pyxis MedStation ES recall
FDA
· CareFusion 303, Inc. · Class II
-
Draeger Vapor 3000. Unheated, calibrated anesthetic vaporizer recall
FDA
· Draeger, Inc. · Class I
-
Draeger Vapor 2000. Unheated, calibrated anesthetic vaporizer recall
FDA
· Draeger, Inc. · Class I
-
Grandma Belle's Tomato Basil Soup, Net Wt recall
FDA
· Lil Turtles LLC · Class II
-
Alinity ci-series System Control Module (SCM) recall
FDA
· Abbott Laboratories · Class II
-
InPen App, Model/CFN Number: MMT-8061 (Android Users) recall
FDA
· Medtronic MiniMed, Inc. · Class II
-
Myosa for Kids KS1 recall
FDA
· Myofunctional Research Company USA · Class II
-
Rocket Product Name: Rocket 20Fg Seldinger Catheter Procedure Tray Model recall
FDA
· Rocket Medical Plc · Class II
-
Rocket Product Name: Rocket 16Fg Seldinger Catheter Procedure Tray Model recall
FDA
· Rocket Medical Plc · Class II
-
Rocket Product Name: Rocket 18Fg Seldinger Catheter with Safety Guard Model recall
FDA
· Rocket Medical Plc · Class II
-
Rocket Product Name: Rocket 18Fg Seldinger Catheter Procedure Tray Model recall
FDA
· Rocket Medical Plc · Class II
-
Rocket Product Name: Rocket 12Fg Seldinger Catheter with Safety Guard Model recall
FDA
· Rocket Medical Plc · Class II
-
Rocket Product Name: Rocket 12Fg Seldinger Catheter Procedure Tray Model recall
FDA
· Rocket Medical Plc · Class II
-
AART Calf Implant Product Name: Calf Implant Model recall
FDA
· Dsaart LLC · Class II
-
AART Pectoral Implant Product Name: Pectoral Implant Model recall
FDA
· Dsaart LLC · Class II
-
AART Malar Implant Product Name: Malar Implant Model recall
FDA
· Dsaart LLC · Class II
-
AART Chin Implant Product Name: Chin Implant Model recall
FDA
· Dsaart LLC · Class II
-
AART Gluteal Implant Product Name: Gluteal Implant Model recall
FDA
· Dsaart LLC · Class II
-
AART Silicone Carving Implant Product Name: Silicone Carving Implant Model recall
FDA
· Dsaart LLC · Class II
-
1ml of DTT in liquid phase, in PET tube with capture cap, in bulk recall
FDA
· Copan Italia · Class II
-
1ml of DTT in liquid phase, in PET tube with capture cap… recall
FDA
· Copan Italia · Class II
-
Intelerad InteleShare software, with ProViewer component recall
FDA
· DICOM Grid, Inc. · Class II
-
Food to Live brand ORGANIC SUPERGREENS POWDER MIX, packaged heat-sealed… recall
FDA
· Lexunder Inc · Class I
-
Food to Live brand ORGANIC MORINGA LEAF POWDER, packaged heat-sealed… recall
FDA
· Lexunder Inc · Class I
-
Hemodialysis System, Surdial DX recall
FDA
· Nipro Medical Corporation · Class II
-
DEXLOCK Achilles Repair Implant Kits, MAKT4520 recall
FDA
· Medline Industries, LP · Class II
-
BD InLay Optima Ureteral Stent Kit Size: 8 Fr recall
FDA
· C.R. Bard Inc · Class II
-
BD InLay Optima Ureteral Stent Kit Size: 6 Fr recall
FDA
· C.R. Bard Inc · Class II
-
BD InLay Optima Ureteral Stent Kit Size: 4.7 Fr recall
FDA
· C.R. Bard Inc · Class II
-
Bard InLay Optima Size: 6 Fr recall
FDA
· C.R. Bard Inc · Class II
-
CONSTRUX" Mini Ti Spacer System Product Name: CONSTRUX" Mini Ti Spacer… recall
FDA
· Orthofix U.S. LLC · Class III
-
Forza" Ti Spacer System Product Name: Forza" Ti Spacer System Model recall
FDA
· Orthofix U.S. LLC · Class III
-
FIREBIRD" SI Fusion System Product Name: FIREBIRD" SI Fusion System Model recall
FDA
· Orthofix U.S. LLC · Class III
-
Pillar" SA PTC Spacer System Product Name: Pillar" SA PTC Spacer System… recall
FDA
· Orthofix U.S. LLC · Class III
-
FORZA" PTC Spacer System Product Name: FORZA" PTC Spacer System Model recall
FDA
· Orthofix U.S. LLC · Class III
-
CONSTRUX" Mini PTC Spacer System Product Name: CONSTRUX" Mini PTC Spacer… recall
FDA
· Orthofix U.S. LLC · Class III
-
ErgoStar CM 60, Model recall
FDA
· Draeger, Inc. · Class I
-
ErgoStar CM 55, Model recall
FDA
· Draeger, Inc. · Class I
-
ErgoStar CM 45, Model recall
FDA
· Draeger, Inc. · Class I
-
ErgoStar CM 40 Model recall
FDA
· Draeger, Inc. · Class I
-
Sticker label (for Loose Bulk - peppermint peaches): 4401 recall
FDA
· Moonlight Packing Corporation · Class I
-
Sticker label (for Loose Bulk - peppermint peaches): 4401 recall
FDA
· Moonlight Packing Corporation · Class I
-
Sticker label (for Loose Bulk - white peaches): 4401 recall
FDA
· Moonlight Packing Corporation · Class I
-
Sticker label (for Loose Bulk - yellow peaches): 4044 recall
FDA
· Moonlight Packing Corporation · Class I
-
Sticker label (for Loose Bulk - yellow peaches): 4044 recall
FDA
· Moonlight Packing Corporation · Class I
-
UPC 8 98429 00266 4 Peppermint Peach PROUCE OF U.S.A. 4 COUNT MIN. WT… recall
FDA
· Moonlight Packing Corporation · Class I
-
UPC 8 10248 03186 1 Peppermint Peach PRODUCE OF U.S.A. NET WT. 2 LBS… recall
FDA
· Moonlight Packing Corporation · Class I
-
UPC 8 10248 03186 1 WHITE PEACHES CALIFORNIA FRUIT PRODUCE OF U.S.A… recall
FDA
· Moonlight Packing Corporation · Class I
-
UPC 8 98429 00209 1 PEACHES PRODUCE OF U.S.A… recall
FDA
· Moonlight Packing Corporation · Class I
-
UPC 8 10248 03087 1 Peppermint Peach WHITE PEACHES READY TO EAT FROM… recall
FDA
· Moonlight Packing Corporation · Class I
-
UPC 8 10248 03165 6 YELLOW Peaches PRODUCE OF U.S.A. NET WT. 4 LBS… recall
FDA
· Moonlight Packing Corporation · Class I
-
Outer-packaging: gimme! brand Decaf de Agua coffee pods, Net Wt recall
FDA
· Gimme Coffee, Inc. · Class II
-
Simplot¿ Traditional Reduced Sodium Tater Gems¿ , formed frozen potatoes… recall
FDA
· JR Simplot Company · Class II
-
Doughy brand Chocolate Chip Cookie Dough recall
FDA
· Hudson River Foods Corp · Class I
-
Lumify Diagnostic Ultrasound System models : 795005, 795161, 989605449841 recall
FDA
· Philips Ultrasound, Inc · Class II
-
Hemochron Activated Clotting Time Low-Range Test Cuvette recall
FDA
· Accriva Diagnostics, Inc. · Class II
-
Phantom Fibula Nail, 2.8mm x 130mm, Right, Ti, Fibula Nail recall
FDA
· Paragon 28, Inc. · Class II
-
Welch Allyn INF BAG, Thigh 1-Tube, Model recall
FDA
· Baxter Healthcare Corporation · Class II