Coaxial Interventional Needle, ITP innotom.com, CE 0297, STERILE EO for the following article numbers: Article no. KIR 23/05, Length 50 mm, Diameter 23 G (0.6 mm); Article no. KIR 23/05N, Length 50 mm, Diameter 23 G (0.6 mm); Article no. KIR 23/07, Length 75 mm, Diameter 23 G (0.6 mm); Article no. KIR 23/07N, Length 70 mm, Diameter 23 G (0.6 mm); Article no. KIR 23/10, Length 100 mm, Diameter 23G (0,6mm); Article no. KIR 23/15, Length 150 mm, Diameter 23 G (0.6 mm); Article no. KIR 21/10, Length 100 mm, Diameter 21 G (0.8 mm); Article no. KIR 21/12, Length 120 mm, Diameter 21 G (0.8 mm); Article no. KIR 21/15, Length 150 mm, Diameter 21 G (0.8 mm); Article no. KIR 21/20, Length 200 mm, Diameter 21 G (0.8 mm); Article no. KIR 17/15, Length 150 mm, Diameter 17 G (1.40mm) Article no. KIR 17/15:45, Length 150 mm, Diameter 17 G (1.40mm) *NOT DISTRIBUTED WITHIN THE US
FDA Recall Z-2163-2021 · Posted None
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Recalling FirmINNOVATIVE TOMOGRAPHY PRODUCT GMBH
Recall StatusOpen, Classified
Product CodeGAA
Date Initiated2021-04-21
Reason for Recall
Sterility Assurance; Coaxial Interventional Needle labeled as sterile may not have been adequately sterilized
Firm Action
On April 20, 2021, Innovative Tomography Products GmbH issued a "urgent Safety Information Product Recall" notification to affected consignees via E-Mail. In addition to informing consignees about the recall products, the firm asked consignees mo to take the following actions:
1. We request that you immediately check your stock of the products in question with the LOT numbers indicated. Please block the corresponding products and quarantine them.
2. Please complete the attached response letter and return it to ITP via E-Mail to the following address:
Address: ITP GmbH
Rckrufunterlagen
Universittsstrae 136
44799 Bochum
Germany
Contact person:
Dominik Frmke
Tel.: +49 234 54621942
Fax: +49 234 54622444
E-Mail: [email protected]
3. Upon receipt of the documents, we will contact you to retrieve and exchange the products.
Information sharing:
4. Please inform all persons within your company belonging to the circle of users about this urgent safety
Root Cause
Vendor change control
Distribution Pattern
US Nationwide distribution in the state of CA.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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