The recalling firm has identified two lots of test strips that are out of specification. Affected test strips show an increased potential for: strip errors prior to applying a blood sample; strips not detected once inserted; or a biased result may occur, which may not be detectable. In the case of a biased result, incorrect action could be taken by the user in response to the displayed blood glucose result as compared to the actual blood glucose value.
All Recalls
95,075 total recalls in our database
A shipment to Guadeloupe suffered a temperature excursions up to 47.8ΒΏC, exceeding the acceptable limits. After detection of the issue, Global Supply Chain QA asked the bioMΒΏrieux distributor in Guadeloupe to put products in quarantine in July 2017; After several reminders, the distributor informed in November 2017 that products were delivered to customers.
Bio-Stable 5F DL-55CM MST-70 KIT Non-Valved PG, Catalog Number 45-871
Angiodynamics Inc. (Navilyst Medical Inc.)
A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens).
XCELA PASV 5F SL 55CM IR-145 Nitinol Wire KIT PG, Catalog Number 25-124
Angiodynamics Inc. (Navilyst Medical Inc.)
A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens).
Bio-Stable 5F SL-55CM IR-145 Kit Valved with Nitinol GW PG, Catalog Number 45-882
Angiodynamics Inc. (Navilyst Medical Inc.)
A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens).
Bio-Stable 5F DL-55CM IR-145 Kit Non-Valved with Nitinol GW PG, Catalog Number 45-887
Angiodynamics Inc. (Navilyst Medical Inc.)
A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens).
RS 5F DL XPP KIT, Catalog Number 60M183104
Angiodynamics Inc. (Navilyst Medical Inc.)
A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens).
The recalling firm identified four US lots of test strips out of specification. Affected strips show increased potential for strip errors prior to applying blood, strips not detected once inserted, or biased results, which may not be detectable. In the case of a biased result, incorrect action could be taken by the user in response to the displayed blood glucose result.
The recalling firm has identified two lots of test strips that are out of specification. Affected test strips show an increased potential for: strip errors prior to applying a blood sample; strips not detected once inserted; or a biased result may occur, which may not be detectable. In the case of a biased result, incorrect action could be taken by the user in response to the displayed blood glucose result as compared to the actual blood glucose value.
12C
Ion Beam Applications S.A.
IBA is initiating this recall to notify its customers that the use of non-IBA accessories and/or third party equipment or unauthorized modifications to an IBA medical device may pose a safety risk.
The High (125 ng/ml) Control does not meet specification - it has been confirmed to produce values below 100 ng/mL when run on validated clinical chemistry analyzers, which is below the 100 ng/mL cutoff of the EDDP Specific Urine Enzyme Immunoassay with which this control is utilized.
A shipment to Guadeloupe suffered a temperature excursions up to 47.8ΒΏC, exceeding the acceptable limits. After detection of the issue, Global Supply Chain QA asked the bioMΒΏrieux distributor in Guadeloupe to put products in quarantine in July 2017; After several reminders, the distributor informed in November 2017 that products were delivered to customers.
Bio-Stable 5F SL-55CM MST-70 Kit Valved with Nitinol Guidewire PG, Catalog Number 45-892
Angiodynamics Inc. (Navilyst Medical Inc.)
A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens).
IBA is recalling to provide information through a Safety Notice to reduce risk for maintenance technicians during ion source replacement.
A shipment to Guadeloupe suffered a temperature excursions up to 47.8ΒΏC, exceeding the acceptable limits. After detection of the issue, Global Supply Chain QA asked the bioMΒΏrieux distributor in Guadeloupe to put products in quarantine in July 2017; After several reminders, the distributor informed in November 2017 that products were delivered to customers.
A shipment to Guadeloupe suffered a temperature excursions up to 47.8ΒΏC, exceeding the acceptable limits. After detection of the issue, Global Supply Chain QA asked the bioMΒΏrieux distributor in Guadeloupe to put products in quarantine in July 2017; After several reminders, the distributor informed in November 2017 that products were delivered to customers.
CAN 5F DL BIOFLO PASV PICC NURSING TRAY, Catalog Number 60M700936
Angiodynamics Inc. (Navilyst Medical Inc.)
A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens).
Brilliance 64 with DEPMED HARDENING KIT 12NC: 459800191351, Model Number 728231. Computed Tomography X-ray system
Philips Medical Systems (Cleveland)
The patient support head holder could contact the back ISO shelter wall during manual or motorized motion through the gantry bore. This may result in a serious injury that would require medical intervention to preclude permanent impairment in certain scenarios.
RS 5F DL BIOFLO PASV, Catalog Number 60M183481
Angiodynamics Inc. (Navilyst Medical Inc.)
A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens).
RS - TANDEM 5F DL BIOFLO MIDLINE, Catalog Number 60M035472
Angiodynamics Inc. (Navilyst Medical Inc.)
A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens).