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FDA (Device enforcement)Recalled 2019-03-14closedclass ii

Nobel Biocare Usa Llc: Implant Retrieval Instrument CC NP & Ext Hex WP 22 mm - Product Usage: They can be used to remove implants, if the implant connection has been damaged. It can be used to remove

Is my product affected?

Implant Retrieval Instrument CC NP & Ext Hex WP 22 mm - Product Usage: They can be used to remove implants, if the implant connection has been damaged. It can be used to remove implants with internal conical connection, internal tri-channel connection or external hex connection.

  • UPC 07332747083798

Check against the official notice below — it lists the full affected range.

What happened

Nobel Biocare USA LLC is recalling 423 units of Implant Retrieval Instrument CC NP & Ext Hex WP 22 mm worldwide, including distribution in the United States and numerous international locations. These instruments are used to remove dental implants when the implant connection has been damaged. The recall was initiated because a problem with the packaging sealing process at the supplier cannot guarantee that the sterilized medical devices will remain sterile throughout their shelf-life.

The affected devices are identified by lot/code information (01)07332747083798(10)73614 and (01)07332747083798(10)73256, with catalog number 37474. The source record does not specify a remedy for affected consumers.

Written by software from the official notice below. Not reviewed by a lawyer.

Hazard

Due to a problem in the packaging sealing process at the supplier of the affected devices, it cannot be guaranteed that the sterilized medical devices in the scope of this recall remain sterile during their shelf-life.

Details from the source

Reason for recall: Due to a problem in the packaging sealing process at the supplier of the affected devices, it cannot be guaranteed that the sterilized medical devices in the scope of this recall remain sterile during their shelf-life. Distribution: Worldwide distribution - US Nationwide distribution and countries of CA, AU, JP, BR, ZA, RU, TW, HK, IN, CN, SA, NZ, MO, CO, LB, AT, BE, CH, CY, DE, DK, EE, ES, FI, FR, GB, GG, GR, HR, HU, IE, LT, LU, NL, PL, PT, RS, SE. Quantity: 423 units Lot/code info: (01)07332747083798(10)73614 (01)07332747083798(10)73256 Catalog# 37474

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.

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