Device recalls

Pacific Hemostasis Thromboplastin-D, 4 ml. Used in performing one-stage prothrombin time test and factor assays.

Fisher Diagnostics · The incorrect value of the International Sensitivity Index (ISI) is printed on the outer box label.

Open, ClassifiedEmployee errorZ-1502-2025
Open FDA's page for this record
Cfres ID
213022
Product res number
Z-1502-2025
Event date initiated
2025-03-06
Event date posted
2025-03-31
Recall status
Open, Classified
Res event number
96488
Product code
GJS
Product description
Pacific Hemostasis Thromboplastin-D, 4 ml. Used in performing one-stage prothrombin time test and factor assays.
Code info
Catalog No. 100356; UDI: 00845275000542719170261130100356; Lot No. 719170; Exp. Date 11/30/26.
Firm FEI number
1181121
Recalling firm
Fisher Diagnostics
Address 1
8365 Valley Pike
City
Middletown
State
VA
Postal code
22645-1905
Additional info contact
Asiyah Imam 800-528-0494
Reason for recall
The incorrect value of the International Sensitivity Index (ISI) is printed on the outer box label.
Root cause description
Employee error
Product quantity
4,387 units
Distribution pattern
US Distribution to: PA and OUS Foreign country of: United Arab Emirates.
Action

A "Recall/Field Safety Corrective Action" letter dated 3/5/25 was mailed to consignees instructing them to stop using and discard any affected product in stock, contact their prescribing physicians/Medical Directors for evaluation for further action, and retain a copy of the notification for laboratory records. Consignees are to return the provided Response Form. Consignees with any questions are to contact their Fisher Diagnostic representative or call 800-528-0494. Distributors are to email techsupport.diagnostics.mtn@thermofisher.com with "CDR-FSN-2025-001" in the subject line to coordinate replacements.

K numbers
K994100
Harmonized identifiers (openFDA)
Device name
Test, Time, Prothrombin
Medical specialty description
Hematology
Regulation number
864.7750
Device class
2
K number
K110212, K213426, K992492, K001699, K904454, K780203, K875062, K093243, K872844, K955843, K791022, K994100, K791023, K961835, K151964, K070005, K931118, K012768, K945078, K892050, K132722, K212779, K974343, K843535, K860721, K092940, K253188, K251564, K060931, K122584, K922565, K180693, K792031, K183255, K071041, K092987, K952608, K170960, K884855, K931117 +87 more
Registration number
2085064, 3037000637, 3013298431, 2432235, 9710666, 3005146313, 3008386529, 3002721930, 9610806, 3006198300, 3012302888, 3010285483, 2245578, 8043723, 3015499222, 1835316, 3030186688, 1181121, 3003691680, 1618982, 3025915415, 2245451, 1217183, 3013188547, 9610126, 3011689956, 3013660430, 3007507465, 1219029, 3033967997, 1832816, 3005643513, 2431530
FEI number
3037000637, 3013298431, 2432235, 3005146313, 3008386529, 3006198300, 3003565434, 3012302888, 3010285483, 3002806559, 3001644026, 2245578, 3001573851, 3015499222, 3030186688, 3000210416, 1181121, 3003691680, 1618982, 1000135102, 2250033, 3025915415, 2245451, 1217183, 3013188547, 3011689956, 3013660430, 3007507465, 1219029, 3033967997, 1832816, 3005643513, 2431530
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.