RecallRadar

FDA Device recall Z-2130-2019

Thyroid Collar Oversize, Product Number TS3, Part Numbers RBTS3-R, RETS3-R, RLTS3-R, RLTS3-SEP, RLTS3-T2T Product Usage: Products are desig…

On 2019-08-07 the FDA classified a Class II recall of Thyroid Collar Oversize, Product Number TS3, Part Numbers RBTS3-R, RETS3-R, RLTS3-R, RLTS3-SEP, RLTS3-T2T Product Usage: Products are desig… by Burlington Medical, citing the protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could expose the user to….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2130-2019
ClassificationClass II
Statusterminated
Initiated2019-06-07
Published2019-08-07
Last updated2026-09-13 11:55 UTC
CompanyBurlington Medical
DistributionUS

Product

Thyroid Collar Oversize, Product Number TS3, Part Numbers RBTS3-R, RETS3-R, RLTS3-R, RLTS3-SEP, RLTS3-T2T Product Usage: Products are designed to protect healthcare workers against scatter (secondary) radiation while performing fluoroscopic and radiographic procedures by reducing the amount of radiation reaching the user.

Reason

The protective material used in the manufacture of the products could potentially provide inadequate protection for the product user. Use of the products could expose the user to scatter radiation of varying degrees depending on many different variables (e.g., distance, shielding, position, time, kV, etc.). Long-term exposure to scatter radiation may increase the risk of cancer, infertility, or other health-related conditions.

Identifiers

code_info
Serial Numbers: 383071 418435 384523 379009 441088 441042 404378 383337 407642 375480 383073 383072 383186…Serial Numbers: 383071 418435 384523 379009 441088 441042 404378 383337 407642 375480 383073 383072 383186 420487 441239 414699 414689 414685 414702 414741 414692 388017 383269

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2130-2019%22

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