SunMed Urgent Medical Device Recall – GreenLine\D Fiber Optic MacIntosh, Size 3 Disposable Laryngoscope Blades
Bound Tree Medical was recently advised about the SunMed Urgent Medical Device Recall for GreenLine\D Fiber Optic MacIntosh, Size 3 Disposable Laryngoscope Blades. The recall is based on a concern of a possible defect of the clear, acrylic light bundle. There is potential for the bundle to break during use.
Urgent Medical Device Recall: One Touch® Ultra® Test Strips
A very small number of OneTouch Ultra Test Strip containers (also called "vials") may contain a hole on the side. This kind of damage to the vial can affect the test strips inside and lead to error messages or blood glucose results that are too high or too low.
Product Recall - Kimberly-Clark/Ballard Medical Products R2 triangle shaped non-radiolucent multifunction electrode products
Bound Tree Medical has received an URGENT: MEDICAL DEVICE RECALL notification from Kimberly-Clark/Ballard Medical Products regarding R2 triangle shaped non-radiolucent multifunction electrode products. This recall affects products that were manufactured prior to June 2005.
FDA and NIOSH Public Health Notification
Oxygen Regulator Fires Resulting from Incorrect Use of CGA 870 Seals. Please see attached for more information.
ACCU-CHECK® Comfort Curve and ACCU-CHECK® Advantage Blood Glucose Test Strips Product Recall
The ACCU-CHECK® Comfort Curve and ACCU-CHECK® Advantage Blood Glucose Test Strips have been recalled due to the potential for wrong results.
Product Recall - ECOTRU® Disinfectant Cleaner (EPA Reg. No. 70791-1)
There has been a product recall for specific lots of ECOTRU® Disinfectant Cleaner (EPA Reg. No. 70791-1) distributed in 2005.
Medical Device Correction – Abbott Blood Glucose Meters
See the attached Medical Device Correction from Abbott Diabetes Care.
Philips Device Correction – HeartStart Pediatric Plus Multifunction Defibrillator Pads
Please be advised of a Device Correction for the Philips HeartStart Pediatric Plus Multifunction Defibrillator Pads. This is a voluntary replacement conducted by Philips Medical Systems involving an “an error on the package label.”
Able Laboratories Recall
Important recall notice for all products under the Able Laboratories, Inc. label. Please click on the link above for more information.
Recall Notice - AccessAED & AccessALS Automated External Defibrillators
Access CardioSystems has issued an urgent recall notice for all AccessAED and AccessALS Automated External Defibrillators. The recall is a result of potential situations in which the device may experience a catastrophic failure of the shock delivery circuit and potential situations in which the device may turn on unexpectedly.
Bound Tree Medical recommends that customers immediately discontinue use and remove from service the items identified in the attached statement.
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