Z-1574-2021Class II
REF CL3960 Oncology Kit w/60" (152 cm) Appx 2.2 ml, Smallbore Ext Set w/w/ChemoLock Port, Clamp, Anti-Siphon...
Abbott Medical / initiated 2021-03-16 / Open, Classified / root cause: design
ICU Medical, Inc. began a recall of REF CL3960 Oncology Kit w/60" (152 cm) Appx 2.2 ml, Smallbore Ext Set w/w/ChemoLock Port, Clamp, Anti-Siphon Valve, Spiros ; w/ChemoLock; Syringe Transfer Set... on . FDA classified it as Class II and gives the reason as "Due to molding defect, there is a potential that certain lots of spinning and non-spinning Sprios male luers may exhibit small amounts of leakage in the inactivated position". As of , the recall status on record is Open, Classified, and MDM tags the root cause as design.
Recall record
- Recall number
- Z-1574-2021
- Classification
- Class II
- Status
- Open, Classified
- Initiated
- Posted
- Recalling firm
- Abbott Medical
- Product
- REF CL3960 Oncology Kit w/60" (152 cm) Appx 2.2 ml, Smallbore Ext Set w/w/ChemoLock Port, Clamp, Anti-Siphon Valve, Spiros ; w/ChemoLock; Syringe Transfer Set w/MicroClave, w/ChemoLock Port - Product Usage: provides access for the administration of fluids from a container to a patient s vascular system through the administration set s needle or catheter (which is inserted into a vein).
- Product code
- ONB Closed Antineoplastic And Hazardous Drug Reconstitution And Transfer System
- Reason for recall
- Due to molding defect, there is a potential that certain lots of spinning and non-spinning Sprios male luers may exhibit small amounts of leakage in the inactivated position.
- Root cause tag
- design
- FDA root cause
- Component design/selection
- Action
- On 03/16/2021, the firm sent an "URGENT: MEDICAL DEVICE RECALL " Letter via Stericycle, Inc. informing customers that it has identified the potential for certain lots of Spiros to exhibit small amounts of leaks due to a molding defect. Customer are instructed to: 1) Discontinue the use and distribution of the affected product immediately. Check their inventory and quarantine all affected product at their facility. 2) Inform potential users of the product in their organization of this notification and complete the attached response form. Return the completed response form to the fax number or e-mail address on the form, even if the customer does not have the affected product. 3) The Recalling Firm has some lots of unaffected product available today and is actively increasing the amount of available inventory. Please contact customer service for product availability. 4) Return affected product using the return label provided with this letter. Contact Stericycle at 1-866-300-2207 (MF, 8am-5pm ET) if customers have not received a return label or require additional labels for returning the affected product. The return labels are for single use only. Do not reproduce. Customers can visit http://expertezlabel.com to request additional labels for returning affected product. To ensure proper and timely credit, follow the instructions on the return label for returning product. Upon receipt of the completed response form and return of the affected product, the Recalling Firm will credit customers for any product returned. Customers will only receive credit for product that are returned. NOTE: Credits for product purchased through distributor will be credited by the distributor. 5) If customers have distributed the product further, immediately notify those accounts that received the product identified in the Affected Product / Table 1 sections of this notification and ask them to contact Stericycle at 1-866-300-2207 (M-F, 8am-5pm ET) to obtain a response form. For
- Distribution
- Worldwide distribution - U.S. Nationwide distribution in the states of AK, AL, AZ, CA, CO, CT, DC, FL, GA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NJ, NV, NY, OH, OK, OR, PA, RI, SD, TN, TX, UT, VA and WA. The countries of Belgium, Canada, France, Italy, South Africa, Spain, United Kingdom.
- Product codes and lots
- REF: CL3960 UDI: (01) 1 0557709 08327 (17) 260101 (30) 50 (10) 5125262 Lot Number: 5125262
Enforcement reports
One row per recalled product line| Recall number | Class | Status | Voluntary or mandated | Report date | Classified |
|---|---|---|---|---|---|
| Z-1565-2021 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-1566-2021 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-1567-2021 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-1568-2021 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-1569-2021 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-1570-2021 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-1571-2021 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-1572-2021 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-1573-2021 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-1574-2021 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-1575-2021 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-1576-2021 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-1577-2021 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-1578-2021 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-1579-2021 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-1580-2021 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-1581-2021 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-1582-2021 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-1583-2021 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-1584-2021 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-1585-2021 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-1586-2021 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-1587-2021 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-1588-2021 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-1589-2021 | Class II | Ongoing | Voluntary: Firm initiated | ||
| Z-1590-2021 | Class II | Ongoing | Voluntary: Firm initiated |
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