Medical device recalls - EOF

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Recall of batches of medical devices: Guedel Airway No. 00 (ISO 5.0) – Code: 1100050, Guedel Airway No. 000 (ISO 3.5) – Code: 1000035

Recall of batches of the medical device “Imager II Angiographic Catheters” of the company BOSTON SCIENTIFIC, class MDD IIa

Recall of batches of polyethylene orthopedic implant components from Howmedica Osteonics Corp.

Recall of batches of medical devices manufactured by BALT EXTRUSION SAS related to ANRYV connectors

Recall of batches of the medical device “BiCOAG hemostatic catheter” of the Olympus company, class MDD IIb

Recall of affected serial numbers, Newport HT70 and HT70 PLUS ventilators and certain related NEWPORT spare parts.

Recall of specific serial numbers of the Bravo CF capsule placement device, product code FGS-0635.

"Recall of batch 240415, expiration date 03/2029 of the medical devices 'X-Glove STERILE SURGICAL GLOVES VIOGLOVE PLUS size 7.0' of VIOLAK INTERNATIONAL SA"

Recall of the batches in the table below of the Medical Device category MDD Class IIb, Smartbag-Liquid Acid Concentrates

Recall of the batches of the following table of the MDD Class IIb Medical Device, OverStritch Suture Cinch and Sature Cinch-Long, (Suture Locking Device and Long Suture Locking Device)

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