-
Medline Convenience Kits: 1) CVC PACK, Model Number: CVI4500A recall
FDA
· Medline Industries, LP · Class II
-
See RES for complete list recall
FDA
· Medline Industries, LP · Class II
-
Medline Convenience Kits: 1) LITHOTOMY PACK, Model Number: DYNJ83185 recall
FDA
· Medline Industries, LP · Class II
-
See RES for complete list recall
FDA
· Medline Industries, LP · Class II
-
See RES for complete list recall
FDA
· Medline Industries, LP · Class II
-
See RES for full list recall
FDA
· Medline Industries, LP · Class II
-
Medline Convenience Kits: 1) DYNDA3003, Model Number: DENTAL PACK recall
FDA
· Medline Industries, LP · Class II
-
Medline Convenience Kits: 1) KIT SURG ONC EXCISION BREAST… recall
FDA
· Medline Industries, LP · Class II
-
Medline Convenience Kits: 1) PICC LINE TRAY, Model Number:00-401993O recall
FDA
· Medline Industries, LP · Class II
-
See RES for complete list recall
FDA
· Medline Industries, LP · Class II
-
Medline Convenience Kits: 1) ANGIO PROCEDURE PACK, Model Number:00-401824AB recall
FDA
· Medline Industries, LP · Class II
-
Medline Convenience Kits: 1) ANGIO PROCEDURE PACK, Model Number:00-401824AA recall
FDA
· Medline Industries, LP · Class II
-
Medline Convenience Kits: 1) SCC RF PAIN MGMT, Model Number:DYNJ56436A recall
FDA
· Medline Industries, LP · Class II
-
Medline Convenience Kits: 1) ANCILLARY PACK-LF, Model Number:DYNJ0185290G recall
FDA
· Medline Industries, LP · Class II
-
One Step P in vitro diagnostic test recall
FDA
· DFI Co., Ltd. · Class II
-
One Step K in vitro diagnostic test recall
FDA
· DFI Co., Ltd. · Class II
-
Uric Acid in vitro diagnostic test recall
FDA
· DFI Co., Ltd. · Class II
-
QUCARE Total Cholesterol in vitro diagnostic test recall
FDA
· DFI Co., Ltd. · Class II
-
One Step pH in vitro diagnostic test recall
FDA
· DFI Co., Ltd. · Class II
-
One Step UTI in vitro diagnostic test recall
FDA
· DFI Co., Ltd. · Class II
-
One Step 10A in vitro diagnostic test recall
FDA
· DFI Co., Ltd. · Class II
-
Biofire Spotfire Respiratory/Sore Throat Panel recall
FDA
· BioFire Diagnostics, LLC · Class II
-
DEX Ophthalmic Tissue Forceps, 27ga DEX Stiff Super Grip Forceps, Model recall
FDA
· Katalyst Surgical, LLC · Class II
-
DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Super Grip Forceps, Model recall
FDA
· Katalyst Surgical, LLC · Class II
-
DEX Ophthalmic Tissue Forceps, 25ga DEX Super Grip Forceps, Model recall
FDA
· Katalyst Surgical, LLC · Class II
-
DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff End Grasping Forceps, Model recall
FDA
· Katalyst Surgical, LLC · Class II
-
DEX Ophthalmic Tissue Forceps, 27ga DEX Stiff Maculorhexis Forceps, Model recall
FDA
· Katalyst Surgical, LLC · Class II
-
DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Maculorhexis Forceps, Model recall
FDA
· Katalyst Surgical, LLC · Class II
-
DEX Ophthalmic Tissue Forceps, 25ga DEX Maculorhexis Forceps, Model recall
FDA
· Katalyst Surgical, LLC · Class II
-
DEX Ophthalmic Tissue Forceps, 23ga DEX Maculorhexis Forceps, Model recall
FDA
· Katalyst Surgical, LLC · Class II
-
DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Serrated Forceps, Model recall
FDA
· Katalyst Surgical, LLC · Class II
-
DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Asymmetrical Tano Forceps… recall
FDA
· Katalyst Surgical, LLC · Class II
-
DEX Ophthalmic Tissue Forceps, 25ga DEX Nano Tapered AWH Forceps, Model recall
FDA
· Katalyst Surgical, LLC · Class II
-
DEX Ophthalmic Tissue Forceps, 23ga DEX NanoTapered AWH Forceps, Model recall
FDA
· Katalyst Surgical, LLC · Class II
-
Mint Lesion recall
FDA
· Mint Medical GmbH · Class II
-
BioFire Joint Infection (JI) Panel recall
FDA
· BioFire Diagnostics, LLC · Class II
-
LIFEPAK 15 recall
FDA
· Physio-Control, Inc. · Class II
-
ERBEFLO 2, Endoscopy Pump Tubing/Cap Set recall
FDA
· Erbe Medical, LLC · Class II
-
ERBEFLO CleverCap: Hybrid Tubing/Cap Set for Olympus Scopes, 20325-201 recall
FDA
· Erbe Medical, LLC · Class II
-
ERBEFLO CleverCap CO2: Hybrid CO2 Tubing/Cap Set for Olympus Scopes & CO2… recall
FDA
· Erbe Medical, LLC · Class II
-
Spacelabs Ultraview SL Command Module Product Name: SL Command Module Model recall
FDA
· Spacelabs Healthcare, Inc. · Class II
-
Prodisc C SK U.S. IMPLANT EXTRA LARGE 6MM. Model Number: PDSXL6… recall
FDA
· Centinel Spine, Inc. · Class II
-
Prodisc C SK U.S. IMPLANT EXTRA LARGE 5MM. Model: PDSXL5 Total cervical… recall
FDA
· Centinel Spine, Inc. · Class II
-
LUX-Dx II Plus, Arrythmia detector and alarm, Model M312… recall
FDA
· Boston Scientific Corporation · Class II
-
LUX-DX II, Arrythmia detector and alarm, Model M302… recall
FDA
· Boston Scientific Corporation · Class II
-
Da Vinci X and Da Vinci Xi Product Name: da Vinci X… recall
FDA
· Intuitive Surgical, Inc. · Class II
-
Medical Action Industries Inc recall
FDA
· Medical Action Industries, Inc. 306 · Class I
-
Convenience kits containing Medline Namic Angiographic Control Syringes… recall
FDA
· American Contract Systems Inc · Class I
-
Halyard VA DETROIT CATH LAB PACK kit recall
FDA
· AVID Medical, Inc. · Class I
-
Halyard SAMMC ANGIOGRAPHY kit recall
FDA
· AVID Medical, Inc. · Class I
-
Halyard PERC TRAY kit recall
FDA
· AVID Medical, Inc. · Class I
-
Halyard NEURO IR PERIPHERAL (PS 64405) kit recall
FDA
· AVID Medical, Inc. · Class I
-
Halyard HEART CATH, SELF REGIONAL kit recall
FDA
· AVID Medical, Inc. · Class I
-
Halyard CATH LAB kit recall
FDA
· AVID Medical, Inc. · Class I
-
Halyard CATH LAB kit recall
FDA
· AVID Medical, Inc. · Class I
-
Halyard CARDIAC CATH TRAY SHANDS JAX kit recall
FDA
· AVID Medical, Inc. · Class I
-
Halyard CARDIAC CATH PACK SAN23CARDQ kit recall
FDA
· AVID Medical, Inc. · Class I
-
Halyard CARDIAC CATH PACK kit recall
FDA
· AVID Medical, Inc. · Class I
-
VOCSN V+Pro package recall
FDA
· Ventec Life Systems, Inc. · Class I
-
Beacon Tip Centimeter Sizing Catheter RPN/GPN NR5.0-35-70-P-10S-0-CSC-20… recall
FDA
· Cook Incorporated · Class I