FDA recall record

INNOVATIVE TOMOGRAPHY PRODUCT GMBH Semi-automatic Biopsy-Needle, ITP innotom.com, CE 0297 recall — FDA Z-2164-2021

Sterility Assurance; Coaxial Interventional Needle labeled as sterile may not have been adequately sterilized

Class IIclassification
Z-2164-2021official record ID
Aug 4, 2021report date

Recall record at a glance

Official recordZ-2164-2021
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmINNOVATIVE TOMOGRAPHY PRODUCT GMBH
Report dateAug 4, 2021
Recall initiation dateApr 21, 2021
QuantityN/A
LocationBochum, N/A, Germany

Official product description

Semi-automatic Biopsy-Needle, ITP innotom.com, CE 0297, STERILE EO for the following article numbers: Article no. BIM 18/10, Length 100 mm, Diameter 18 G (1.25 mm); Article no. BIM 18/15, Length 150 mm, Diameter 18 G (1.25 mm); Article no. BIM 18/20, Length 200 mm, Diameter 18 G (1.25 mm); Article no. BIM 16/10, Length 100 mm, Diameter 16 G (1.6 mm); Article no. BIM 16/15, Length 150 mm, Diameter 16 G (1.6 mm); Article no. BIM 16/20, Length 200 mm, Diameter 16 G (1.6 mm); Article no. BIM 14/10, Length 100 mm, Diameter 14 G (2.1 mm); Article no. BIM 14/15, Length 150 mm, Diameter 14 G (2.1 mm); Article no. BIM 14/20, Length 200 mm, Diameter 14 G (2.1 mm) *NOT DISTRIBUTED WITHIN THE US

Why the product was recalled

Sterility Assurance; Coaxial Interventional Needle labeled as sterile may not have been adequately sterilized

Distribution information

US Nationwide distribution in the state of CA.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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