-
UNiD" Adaptive Spine Intelligence UNiD Spine Analyzer Product Number… recall
FDA
· Medicrea International · Class II
-
Beckman Coulter DxI 9000 Access Immunoassay Analyzer, catalog number C11137 recall
FDA
· Beckman Coulter, Inc. · Class II
-
Brasseler ESR Rotary/Reciprocating Endodontic File Device SKU AP120213PK… recall
FDA
· US Endodontics, LLC · Class II
-
Sysmex PS-10 Sample Preparation System with software version 1.5 and 1.6 recall
FDA
· Sysmex America, Inc. · Class II
-
Access PCT Reagent Pack recall
FDA
· Beckman Coulter, Inc. · Class II
-
Temporary Titanium Abutments recall
FDA
· DDS Lab · Class II
-
IntelliVue Patient Monitor MX550. Model Number: 866066 recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Patient Monitor MX500. Model Number: 866064 recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Patient Monitor MX450. Model Number: 866062 recall
FDA
· Philips North America Llc · Class II
-
IntelliVue Patient Monitor MX400. Model Number: 866060 recall
FDA
· Philips North America Llc · Class II
-
IntelliBridge EC10 Module recall
FDA
· Philips North America Llc · Class II
-
NeiMed NasoGel for DRY NOSES UDI-DI recall
FDA
· Neilmed Pharmaceuticals Inc · Class II
-
Integra Miltex Cryosolutions Cartridges 4 Pack (23.5g N2O each)… recall
FDA
· New Medical Technologies Gmbh · Class II
-
Integra Miltex CryoSolutions Cartridges 10 Pack (23.5g N2O each)… recall
FDA
· New Medical Technologies Gmbh · Class II
-
LIFEPAK 35 ECG cable recall
FDA
· Physio-Control, Inc. · Class II
-
Nobel Biocare N1 TiUltra TCC RP 4.0x9mm . Nobel Biocare N1 TiUltra TCC RP… recall
FDA
· Nobel Biocare · Class II
-
Belmont Medical 3-Spike Disposable Set used with the Belmont Rapid Infuser… recall
FDA
· Belmont Instrument LLC · Class II
-
ETHIBOND EXCEL Polyester Suture recall
FDA
· Ethicon, LLC · Class II
-
PERMA-HAND Silk Suture recall
FDA
· Ethicon, LLC · Class II
-
PROLENE Polypropylene Suture recall
FDA
· Ethicon, LLC · Class II
-
The Rapid fFN Specimen Collection Tube (PN: 71550-001) is a component of… recall
FDA
· Hologic, Inc · Class II
-
Azurion 7 M20 System code: (1) 722224 (2) 722079 (3) 722234 (4) 722282… recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Azurion 7 M12 System Code: (1) 722078 (2) 722223 (3) 722233 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Azurion 7 B20 System Code: (1) 722068 (2) 722226 (3) 722236 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Azurion 7 B12 System Code: (1) 722067 (2) 722225 (3) 722235 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Azurion 5 M20 System Code: (1) 722228 (2) 722232 (3) 722281 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Azurion 5 M12 System Code: (1) 722227 (2) 722231 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Azurion 3 M15 System Code: (1) 722064 (2) 722222 (3) 722280 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Azurion 3 M12 System Code: (1) 722063 (2) 722221 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
AlluraXperFD20/15 System Code: (1) 722058 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD20/20 System Code: (1) 722038 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
AlluraXperFD20/10 System Code: (1) 722029 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
AlluraXper FD20 OR Table System Code: (1) 722023 (2) 722035 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
AlluraXper FD20 Biplane OR Table System Code: (1) 722020 (2) 722025 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
AlluraXper FD20 Biplane System Code: (1) 722008 (2) 722013 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
AlluraXper FD20 System Code: (1) 722006 (2) 722012 (3) 722028 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD10C System Code: (1) 722001 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
AlluraXper FD10/10 System Code: (1) 722005 (2) 722011 (3) 722027 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura Xper FD10 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Allura CV20 System Code: 722031 recall
FDA
· Philips Medical Systems Nederland B.V. · Class II
-
Lev5, REF CT1587B, 50 Susceptibility discs Levofloxacin 5 ug, IVD, CE 2797 recall
FDA
· Oxoid Limited · Class II
-
SenTiva, REF: 1000C, Generators Part of the VNS Therapy System with… recall
FDA
· LivaNova USA, Inc. · Class II
-
SenTiva, REF: 1000; SenTiva Duo, REF: 1000-D… recall
FDA
· LivaNova USA, Inc. · Class II
-
regard Item Number: 830106006, LD01114F - Newborn Kit containing the… recall
FDA
· ROi CPS LLC · Class I
-
Optima XR646 HD. X-Ray imaging system recall
FDA
· GE Medical Systems, LLC · Class II
-
Discovery XR656 HD. X-Ray imaging system recall
FDA
· GE Medical Systems, LLC · Class II
-
Discovery XR656HD. X-Ray imaging system recall
FDA
· GE Medical Systems, LLC · Class II
-
Definium 656HD & Discovery XR656HD (GTINs: 00840682138598, 00195278840226… recall
FDA
· GE Medical Systems, LLC · Class II
-
Ivenix Infusion System (IIS), LVP Software LVP-SW-0005… recall
FDA
· Fresenius Kabi USA, LLC · Class I
-
Product is individually packaged in opaque airtight plastic packaging with… recall
FDA
· Mutual Trading Company Inc. · Class I
-
La Fiesta PAN RAYADO SAZONADO Bread Crumbs Seasoned, NET WT 8 OZ. (227g) recall
FDA
· La Fiesta Food Products · Class I
-
La Fiesta PAN RAYADO Bread Crumbs, NET WT 8 OZ. (227g) recall
FDA
· La Fiesta Food Products · Class I
-
COLUSSI CANTUCCINI CHOCOLATE DROPS COOKIES recall
FDA
· D. Coluccio & Sons Inc. · Class II
-
White Maeng da, kratom powder product packaged mylar resealable bags recall
FDA
· Corepack Manufacturing Inc · Class I
-
item 8202891 PLAIN VANILLA MINI CAKE DONUT RING BULK 240X1.25OZ… recall
FDA
· Fgf, LLC · Class II
-
item 8202731 UNFLD BISMARK DONUT PFD 78X3OZ, NET WT 13.16 LB recall
FDA
· Fgf, LLC · Class II
-
item 8201936 NATURAL & ARTIFICIAL FLAVORED BAVARIAN BISMARK… recall
FDA
· Fgf, LLC · Class II
-
item 8201927 APPLE FRITTER DONUT PFD 70 X 3.5OZ, NET WT 13.78 LB recall
FDA
· Fgf, LLC · Class II
-
item 8201926 FBALL/EGG SHPD DONUT PFD 78 X 2OZ, NET WT 8.78 LB recall
FDA
· Fgf, LLC · Class II
-
item 8201923 BAV CRM BAR DONUT PFD 78 X 3OZ, NET WT 13.16 LB recall
FDA
· Fgf, LLC · Class II