PANTHER FUSION System REF 9121010000 The Panther System is an integrated nucleic acid testing system which fully automates all steps necessary to perform Aptima assays from sample processing through amplification, detection, and data reduction. The Panther Fusion System is an integrated, fully automated, in vitro diagnostic (IVD) clinical multiplex test system. It is capable of performing nucleic acid based tests from sample processing through amplification, detection, and data reduction.

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Fusion System Part Number: ASY-09600 UDI Code: Pending Serial Numbers Panther / Fusion: 1010910036 2101000822 1010910056 2101000883 1010910064 2101000783 1010910075 2101000786 1010910111 2101000654 1010910171 2101000961 1010910195 2101000810 1010910216 2101000866 1010910220 2101000500 1010910343 2101000779 1010910389 2101000901 1010910453 2101000900 1010910461 2101000675 1010910470 2101000645 1010910504 2101000674 1010910544 2101000703 1010910551 2101001001 1010910571 2101000837 1010910647 2101000893 1010910649 2101000712 1010910672 2101000760 1010910686 2101000979 1010910690 2101000775 1010910691 2101000778 1010910716 2101000845 1010910731 2101000827 1010910732 2101000831 1010910733 2101000807 1010910789 2101000858 1010910790 2101000859 1010910795 2101000879 1010910821 2101000894 1010910824 2101000916 1010910825 2101000917 1010910826 2101000919 1010910837 2101000846 1010910856 2101000939 1010910877 2101000947 2090000355 2101000218 2090000527 2101000791 2090000585 2102100927 2090000617 2101000355 2090000747 2101000655 2090000798 2101000344 2090000896 2101000885 2090000902 2101000918 2090000909 2101000236 2090000959 2101000414 2090000996 2101000334 2090001017 2101000834 2090001099 2101000079 2090001309 2101000083 2090001393 2101000214 2090001410 2101000119 2090001424 2101000324 2090001550 2101000889 2090001556 2101000973 2090001591 2101000075 2090001656 2101000860 2090001700 2101000902 2090001740 2101000888 2090001780 2101000994 2090001786 2101000139 2090001860 2101000577 2090001871 2101000616 2090001872 2101000173 2090001886 2101000310 2090002308 2101001008 2090002339 2101000128 2090002341 2101000376 2090002447 2101000374 2090002462 2101000777 2090002487 2101000459 2090002530 2101000785 2090002551 2101000231 2090002572 2101000136 2090002692 2101000273 2090002730 2101000342 2090002742 2101000312 2090002768 2101000833 2090002798 2101000118 2090002810 2101000895 2090002824 2101000248 2090002847 2101000225 2090002911 2101000773 2090002964 2101000252 2090002969 2101000890 2090002976 2101000816 2090003009 2101000474 2090003024 2101000993 2090003100 2101000821 2090003101 2101000830 2090003110 2101000946 2090003126 2101000288 2090003170 2101000670 2090003245 2101000865 2090003248 2101000285 2090003314 2101000333 2090003315 2101000341 2090003318 2101000353 2090003326 2101000308 2090003358 2101000360 2090003379 2101000817 2090003384 2101000820 2090003390 2101000715 2090003394 2101000792 2090003415 2101000343 2090003456 2101000350 2090003540 2101000397 2090003551 2101000418 2090003553 2101000385 2090003555 2101000403 2090003556 2101000608 2090003574 2101000421 2090003658 2101000440 2090003672 2101000716 2090003674 2101000451 2090003739 2101000835 2090003805 2101000829 2090003818 2101000480 2090003819 2101000482 2090003820 2101000794 2090003822 2101000468 2090003922 2101000823 2090003941 2101000793 2090004065 2101000579 2090004138 2101000705 2090004188 2101000656 2090004224 2101000824 2090004229 2101000825 2090004299 2101000795 2090004300 2101000796 2090004389 2101000782 2090004412 2101000808 2090004414 2101000891
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Hologic, Inc.
Reason for Recall:
Due to potential false positive Flu B results when a sample was also SARS-CoV-2 positive.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

PANTHER FUSION System REF 9121010000 The Panther System is an integrated nucleic acid testing system which fully automates all steps necessary to perform Aptima assays from sample processing through amplification, detection, and data reduction. The Panther Fusion System is an integrated, fully automated, in vitro diagnostic (IVD) clinical multiplex test system. It is capable of performing nucleic acid based tests from sample processing through amplification, detection, and data reduction.

Product Codes/Lot Numbers:

Fusion System Part Number: ASY-09600 UDI Code: Pending Serial Numbers Panther / Fusion: 1010910036 2101000822 1010910056 2101000883 1010910064 2101000783 1010910075 2101000786 1010910111 2101000654 1010910171 2101000961 1010910195 2101000810 1010910216 2101000866 1010910220 2101000500 1010910343 2101000779 1010910389 2101000901 1010910453 2101000900 1010910461 2101000675 1010910470 2101000645 1010910504 2101000674 1010910544 2101000703 1010910551 2101001001 1010910571 2101000837 1010910647 2101000893 1010910649 2101000712 1010910672 2101000760 1010910686 2101000979 1010910690 2101000775 1010910691 2101000778 1010910716 2101000845 1010910731 2101000827 1010910732 2101000831 1010910733 2101000807 1010910789 2101000858 1010910790 2101000859 1010910795 2101000879 1010910821 2101000894 1010910824 2101000916 1010910825 2101000917 1010910826 2101000919 1010910837 2101000846 1010910856 2101000939 1010910877 2101000947 2090000355 2101000218 2090000527 2101000791 2090000585 2102100927 2090000617 2101000355 2090000747 2101000655 2090000798 2101000344 2090000896 2101000885 2090000902 2101000918 2090000909 2101000236 2090000959 2101000414 2090000996 2101000334 2090001017 2101000834 2090001099 2101000079 2090001309 2101000083 2090001393 2101000214 2090001410 2101000119 2090001424 2101000324 2090001550 2101000889 2090001556 2101000973 2090001591 2101000075 2090001656 2101000860 2090001700 2101000902 2090001740 2101000888 2090001780 2101000994 2090001786 2101000139 2090001860 2101000577 2090001871 2101000616 2090001872 2101000173 2090001886 2101000310 2090002308 2101001008 2090002339 2101000128 2090002341 2101000376 2090002447 2101000374 2090002462 2101000777 2090002487 2101000459 2090002530 2101000785 2090002551 2101000231 2090002572 2101000136 2090002692 2101000273 2090002730 2101000342 2090002742 2101000312 2090002768 2101000833 2090002798 2101000118 2090002810 2101000895 2090002824 2101000248 2090002847 2101000225 2090002911 2101000773 2090002964 2101000252 2090002969 2101000890 2090002976 2101000816 2090003009 2101000474 2090003024 2101000993 2090003100 2101000821 2090003101 2101000830 2090003110 2101000946 2090003126 2101000288 2090003170 2101000670 2090003245 2101000865 2090003248 2101000285 2090003314 2101000333 2090003315 2101000341 2090003318 2101000353 2090003326 2101000308 2090003358 2101000360 2090003379 2101000817 2090003384 2101000820 2090003390 2101000715 2090003394 2101000792 2090003415 2101000343 2090003456 2101000350 2090003540 2101000397 2090003551 2101000418 2090003553 2101000385 2090003555 2101000403 2090003556 2101000608 2090003574 2101000421 2090003658 2101000440 2090003672 2101000716 2090003674 2101000451 2090003739 2101000835 2090003805 2101000829 2090003818 2101000480 2090003819 2101000482 2090003820 2101000794 2090003822 2101000468 2090003922 2101000823 2090003941 2101000793 2090004065 2101000579 2090004138 2101000705 2090004188 2101000656 2090004224 2101000824 2090004229 2101000825 2090004299 2101000795 2090004300 2101000796 2090004389 2101000782 2090004412 2101000808 2090004414 2101000891

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0782-2024

Related Recalls

Three lots of Rapid fFN Specimen Collection kit (901164, 901165, and 904850) contain Rapid fFN Specimen Collection Tubes which may be empty, underfilled, or overfilled with extraction buffer. The transport tubes are used with the Fetal Fibronectin Enzyme Immunoassay and Rapid fFNΒΏ for the TLiIQΒΏ System which aids in assessing the risk of preterm delivery. The use of empty transport tubes or transport tubes containing insufficient extraction buffer volume may result in invalid results and/or delays in obtaining results. Additionally, the use of underfilled tubes may result in false positive results and the use of overfilled tubes may result in false negative results.

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