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FDA (Device enforcement)Recalled 2021-12-06closedclass ii

Abbott Molecular, Inc.: Alinity m System, Part No. 08N53-002

Is my product affected?

Alinity m System, Part No. 08N53-002

  • UPC 00884999048034

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

What happened

Abbott Molecular, Inc. is recalling 74 Alinity m System devices (Model 08N53-002) due to an issue with the installation of updated camera firmware on the system. The affected devices were distributed in the United States across California, Washington DC, Georgia, Kentucky, Illinois, Maryland, Michigan, Minnesota, Mississippi, New Hampshire, New Jersey, New York, Rhode Island, South Dakota, Texas, and Wisconsin, as well as internationally to Australia, Cambodia, Canada, Colombia, France, Germany, Israel, Italy, Malaysia, Mozambique, Portugal, South Africa, Spain, Switzerland, Taiwan, the United Kingdom, and Vietnam.

Consumers who believe they have one of the affected devices can identify it by checking whether their Alinity m System serial number matches one of the 74 listed impacted serial numbers (ranging from 00048 to 00712). The recall record does not specify what remedy is available to consumers or what actions they should take.

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

Hazard

There is an issue with the installation of updated camera firmware on the system.

Details from the source

Reason for recall: There is an issue with the installation of updated camera firmware on the system. Distribution: Distribution in the United States in CA, DC, GA, KY, IL, MD, MI, MN, MS, NH, NJ, NY, RI, SD, TX, WI OUS distribution to Australia, Cambodia, Canada, Columbia, France, Germany, Israel, Italy, Malaysia, Mozambique, Portugal, South Africa, Spain, Switzerland, Taiwan, United Kingdom, and Vietnam Quantity: 74 devices Lot/code info: Alinity m System, Model 08N53-002 74 impacted serial numbers: 00048, 00076, 00080, 00091, 00105, 00111, 00154, 00155, 00165, 00189, 00191, 00207, 00231, 00232, 00233, 00239, 00252, 00254, 00267, 00280, 00284, 00285, 00288, 00290, 00292, 00293, 00294, 00296, 00302, 00320, 00331, 00343, 00345, 00348, 00357, 00376, 00416, 00418, 00430, 00437, 00466, 00474, 00485, 00486, 00495, 00537, 00540, 00541, 00554, 00566, 00598, 00624, 00629, 00641, 00652, 00656, 00673, 00696, 00697, 00698, 00699, 00700, 00701, 00702, 00703, 00704, 00705, 00706, 00707, 00708, 00709, 00710, 00711, 00712 Impacted UDI numbers: (01)00884999048034(11)190115(21)00048(240)08N53-002 (01)00884999048034(11)190326(21)00076(240)08N53-002 (01)00884999048034(11)190331(21)00080(240)08N53-002 (01)00884999048034(11)190423(21)00091(240)08N53-002 (01)00884999048034(11)190523(21)00105(240)08N53-002 (01)00884999048034(11)190522(21)00111(240)08N53-002 (01)00884999048034(11)190807(21)00154(240)08N53-002 (01)00884999048034(11)190809(21)00155(240)08N53-002 (01)00884999048034(11)190822(21)00165(240)08N53-002 (01)00884999048034(11)191001(21)00189(240)08N53-002 (01)00884999048034(11)191003(21)00191(240)08N53-002 (01)00884999048034(11)191105(21)00207(240)08N53-002 (01)00884999048034(11)200107(21)00231(240)08N53-002 (01)00884999048034(11)200113(21)00232(240)08N53-002 (01)00884999048034(11)200123(21)00233(240)08N53-002 (01)00884999048034(11)200130(21)00239(240)08N53-002 (01)00884999048034(11)200220(21)00252(240)08N53-002 (01)00884999048

Source

Official record: FDA (Device enforcement) ↗

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

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