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All product recalls associated with Exactech, Inc..
Total Recalls
1000
Past Year
1000
Class I (Serious)
143
Most Recent
Jan 2026
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
An implant within a lot of finned tibial trays manufactured at Exactech was not made to specification. The locking cavity in the tibial tray was not fully machined thus preventing the tibial insert from locking in place.
The recalled batteries were sold with the following Dell notebook computers: Latitude™ D410, D505, D510, D600, D610, D800, D810; Inspiron™ 510M, 600M, 6000, 8600, 9200, 9300, XPS Gen 2; and Dell Precision™ M20 and M70 mobile workstations. The batteries were also sold separately, including as secondary batteries and in response to service calls. The batteries insert into the battery bay located on the underside of the notebook. "Dell" and "Made in Japan" or "Made in China" are stamped on the batteries. The identification number for each battery appears on a white sticker. Customers should have this number available when they contact Dell to determine if their battery is part of the recall.
T-Cell test results and the respective absolute counts for the CELL-DYN Sapphire instrument using CD3/4/8 reagents can be overestimated by as much as 13%.
Software error may report higher results for glucose and lactate
Sterility is compromised by incomplete package seal.
Sterility is compromised by incomplete package seal.
Firm received one report of a false negative with the positive control. Internal testing by the firm has shown that the kit lot may result in invalid or false negative interpretations.
The extension sets contain microbore female luers that may crack during use, resulting in leakage of medication or incomplete delivery of medication.
The extension sets contain microbore female luers that may crack during use, resulting in leakage of medication or incomplete delivery of medication.
The recalled GE Monogram built-in ranges include models ZDP48N6RH1SS, ZDP48L6RH1SS, ZDP48N4GH1SS, ZDP48L4GH1SS, ZDP48N6DH1SS, ZDP48L6DH1SS, ZDP36N4DH1SS, and ZDP36L4DH1SS. The recalled ranges have serial numbers starting with DG, FG, GG, HG, LG, MG, RG, SG, TG, VG, ZG, AH, DH, FH, GH, HH, LH, MH, RH, SH. To find the model and serial number, look underneath the top ledge (also called the "bull nose"), above the range controls. They were manufactured from February 1, 2004 to October 1, 2005.
The extension sets contain microbore female luers that may crack during use, resulting in leakage of medication or incomplete delivery of medication.
There is a risk of sample misidentification when processing samples in the Manual aspiration mode.
The extension sets contain microbore female luers that may crack during use, resulting in leakage of medication or incomplete delivery of medication.
The extension sets contain microbore female luers that may crack during use, resulting in leakage of medication or incomplete delivery of medication.
The extension sets contain microbore female luers that may crack during use, resulting in leakage of medication or incomplete delivery of medication.
The extension sets contain microbore female luers that may crack during use, resulting in leakage of medication or incomplete delivery of medication.
The extension sets contain microbore female luers that may crack during use, resulting in leakage of medication or incomplete delivery of medication.
The extension sets contain microbore female luers that may crack during use, resulting in leakage of medication or incomplete delivery of medication.
The extension sets contain microbore female luers that may crack during use, resulting in leakage of medication or incomplete delivery of medication.
The extension sets contain microbore female luers that may crack during use, resulting in leakage of medication or incomplete delivery of medication.