|
Product Description
|
Recall Class
|
FDA Recall Posting Date
|
Recalling Firm
|
K-204 GUIDE SHEATH Kit 2.6MM, model no K-204 - Product Usage: Used with endoscopes to collect cells ...
|
2
|
02/05/2021
|
Aomori Olympus Co., Ltd.
|
K-202 GUIDE SHEATH KIT 2.0MM, model no. K-202 - Product Usage: Used with endoscopes to collect cells...
|
2
|
02/05/2021
|
Aomori Olympus Co., Ltd.
|
K-203 GUIDE SHEATH KIT 2.6MM, model no. K-203 - Product Usage: Used with endoscopes to collect cells...
|
2
|
02/05/2021
|
Aomori Olympus Co., Ltd.
|
K-204 GUIDE SHEATH KIT 2.6MM, model no. K-204 - Product Usage: Used with endoscopes to collect cells...
|
2
|
02/05/2021
|
Aomori Olympus Co., Ltd.
|
K-202 GUIDE SHEATH Kit 2.0MM, model no. K-202 - Product Usage: Used with endoscopes to collect cells...
|
2
|
02/05/2021
|
Aomori Olympus Co., Ltd.
|
K-201 GUIDE SHEATH Kit 2.0MM, model no. K-201 - Product Usage: Used with endoscopes to collect cells...
|
2
|
02/05/2021
|
Aomori Olympus Co., Ltd.
|
K-201 GUIDE SHEATH KIT 2.0MM, model no. K-201 - Product Usage: Used with endoscopes to collect cells...
|
2
|
02/05/2021
|
Aomori Olympus Co., Ltd.
|
Box Label: ION Fully Articulating Catheter, REF 490105, VER 08 - Product Usage: used to navigate the...
|
2
|
11/25/2020
|
Intuitive Surgical, Inc.
|
Olympus Medical Systems Corporation (OMSC) Evis Exera II Bronchovideoscope Olympus BF Type Q180 (BF-...
|
2
|
09/25/2020
|
Olympus Corporation of the Americas
|
ION Reprocessing Accessories Kit, IF1000 (Part Number: 490024-03) UDI:00886874119129. The kit includ...
|
2
|
09/10/2020
|
Intuitive Surgical, Inc.
|