Bd Syringe Recall at Jonathan Middleton blog

Bd Syringe Recall. for questions pertaining to a specific medical device recall, please see the contact information within the product recall. the recall affects model numbers 8110, 8015 and 8120. Bd distributed affected devices between june 19, 2004, and sept. Bd initiated the recall on sept. bd has confirmed that one lot of the bd™ syringe tip cap bulk sterile convenience pak exhibits holes in product packaging,. bd has identified an increase in bent contacts on new female/left iui connectors on devices and spare parts. To date, the recall has affected 220,120 syringe pump and pca modules and 867,362 pcu modules. For questions pertaining to a specific medical device recall, please see the contact information within the. bd/carefusion 303 is recalling their alaris infusion pumps to make a correction on compatibility issues with. the affected products were manufactured using unvalidated materials that can result in unsealed packaging for.

BD Syringes Luer Lock Consumer's Choice Medical
from consumerschoicemedical.com

bd has identified an increase in bent contacts on new female/left iui connectors on devices and spare parts. for questions pertaining to a specific medical device recall, please see the contact information within the product recall. bd/carefusion 303 is recalling their alaris infusion pumps to make a correction on compatibility issues with. For questions pertaining to a specific medical device recall, please see the contact information within the. bd has confirmed that one lot of the bd™ syringe tip cap bulk sterile convenience pak exhibits holes in product packaging,. the affected products were manufactured using unvalidated materials that can result in unsealed packaging for. Bd initiated the recall on sept. Bd distributed affected devices between june 19, 2004, and sept. the recall affects model numbers 8110, 8015 and 8120. To date, the recall has affected 220,120 syringe pump and pca modules and 867,362 pcu modules.

BD Syringes Luer Lock Consumer's Choice Medical

Bd Syringe Recall Bd distributed affected devices between june 19, 2004, and sept. For questions pertaining to a specific medical device recall, please see the contact information within the. To date, the recall has affected 220,120 syringe pump and pca modules and 867,362 pcu modules. Bd distributed affected devices between june 19, 2004, and sept. the recall affects model numbers 8110, 8015 and 8120. the affected products were manufactured using unvalidated materials that can result in unsealed packaging for. Bd initiated the recall on sept. bd has identified an increase in bent contacts on new female/left iui connectors on devices and spare parts. bd/carefusion 303 is recalling their alaris infusion pumps to make a correction on compatibility issues with. for questions pertaining to a specific medical device recall, please see the contact information within the product recall. bd has confirmed that one lot of the bd™ syringe tip cap bulk sterile convenience pak exhibits holes in product packaging,.

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