Medical Device Recall: Z-0017-2020

FDA Recalls dataset · Firm: Inter-Med Llc · Status: Terminated

Recall Action Class: N/A Date Initiated: 2019-06-27 Recall record compiled from public FDA source records.

Recall Parameters & Description

Normalized public record details for FDA recall code Z-0017-2020.

Recall Res Number
Z-0017-2020
Recalling Firm / Manufacturer
FEI Number
3000209941
Recall Status
Terminated
Recall Classification
N/A
Date Initiated
2019-06-27
Date Posted
2019-10-01
Date Terminated
2021-08-10
Product Code
KJJ
Event Number
83435
Product Quantity
384 units
Product Description Vista Dental Products Chlor-XTRA - 12mL Prefilled Syringes, QTY: 8, REF 503850

Reason for Recall The affected lots may be packaged in syringes which include an incorrect bung. The incorrect bung is made of a latex-free isoprene rubber material. After prolonged storage and exposure to contained solutions, the rubber bung may degrade due to chemical interaction with the bleach solution.

Action Details The firm initiated the recall by letter on 06/27/2019. The letter directed the consignee to quarantine the product and contact the returns department for return instructions.

Distribution Pattern US, South Africa, Switzerland, Poland, Italy, Singapore, Australia

Code Information / Serial Numbers Lot/Work Order Numbers: 2018-1471 2018-1992 20182211, UDI (01)10818207020502 20182779, UDI (01)10818207020502 20190041, UDI (01)10818207020502 20190309, UDI (01)10818207020502

Related Establishments / Registrations

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This page represents an index of public-record FDA device recalls. It does not imply current safety or compliance status of the product. AvaSpecs is a private aggregator and is not affiliated with the FDA or any government agency. This page does not constitute medical, safety, legal, regulatory, or compliance advice. Refer to official government sources for primary safety alerts.

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