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