Bioseal, Central Line Dressing Kit, containing ChloraPREP Applicator 3 mL, REF: CVC015/20, Sterile EO, UDI: (01)00630094430157
FDA Recall Z-1622-2021 · Posted None
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Recalling FirmBioseal Corporation
Recall StatusCompleted
Product CodeKDD
Date Initiated2021-03-23
Product Quantity1,560 units
Reason for Recall
Pre-op skin prep component ChloraPrep included within kits may allow the growth of Aspergillus penicillioides, which may penetrate the packaging resulting in a breach of the package integrity.
Firm Action
On 3/23/21, Bioseal emailed an "Urgent: Medical Device Recall" notice to affected consignees. In addition to informing consignees about the recall the firm ask consignees to take the following actions:
1. Please discontinue use of the product listed above.
2. Please complete enclosed response form listing the quantity of affected product on hand via email to [email protected]. Even if you do not have the affected product please complete and return the form. Once we have received the completed form we will forward product return information, if applicable.
3. If you have transferred possession of the product to another organization, you are required by FDA regulations to notify them of this recall communication. Please have any affected product returned to you for collection and return to Bioseal as specified above.
4. Adverse reactions or quality problems experience with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program.
5. If you have any questions regarding this matter, please contact customer service at 800-441-7325, Monday-Friday 8:00 AM - 5:00 PM P.S.T.
Root Cause
Unknown/Undetermined by firm
Distribution Pattern
US: IL and MO OUS: None
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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