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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: BIOMERIEUX INC. AST-ST03 TEST KIT 20 CARDS

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BIOMERIEUX INC. AST-ST03 TEST KIT 20 CARDS Back to Search Results
Catalog Number 421040
Device Problem Low Test Results (2458)
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Type  malfunction  
Event Description
Intended use: the vitek® 2 streptococcus susceptibility card is intended for use with the vitek® 2 systems in clinical laboratories as an in vitro test to determine the susceptibility of s.Pneumoniae, beta-hemolytic streptococcus, and viridans streptococcus to antimicrobial agents when used as instructed.Issue description: a customer from spain notified biomérieux of false susceptible trimethoprim/sulfamethoxazole (sxt) for streptococcus agalactiae - (group b) patient strain in association with vitek 2 ast-st03 test kit (ref: (b)(4), lot: 5422257203, expiration date 1/31/2024).This complaint is related to complaint: (b)(4) (same patient, same issue, different product: ast-p589 test kit).The two complaints (b)(4), this complaint) were created to document ast results obtained with samples from a patient with a finger injury: (b)(4) (same patient, same issue, different product: ast-p589 test kit: 22279) documents a potential false resistant sxt result which could have contributed to additional interventions for the patient, including the loss of part of the patient¿s finger.This complaint was reported as a potential serious injury (reference: 1950204-2023-00001).Complaint (b)(4) documents a false resistant result which was not reported and was obtained in the context of off-label use.Patient¿s history: the patient is a woman, 32 years old, that had three (3) surgeries on the finger wound and has lost some of the ring finger due to infection.The patient is not responding to treatment and is allergic to beta-lactam antibiotics and vancomycin, so treatment options are limited.The patient was treated with cotrimoxazole in september and october 2022 prior to sending the first sample to the laboratory.Currently the patient is on cycles of cotrimoxazole and linezolid.Information on ast results: in october, the customer analyzed a first sample (swab from the wound) with vitek 2 (ast-p589 test kit: 22279), which reported sxt susceptible for s.Agalactiae.Sxt treatment was initiated, but was unsuccessful in eliminating the infection.Between october 2022 and february 2023, samples from this patient continued to arrive at the laboratory, including tissue from two (2) interventions that the patient had to undergo for the infection (part of the finger was removed).Testing reported positive for s.Agalactiae and susceptible to sxt (test methods performed were not disclosed by the customer).Finally, in february 2023, since the patient did not respond favorably to the treatment, the customer performed testing with the vitek 2 ast-st03 card (results documented in this complaint (b)(4), disk diffusion and etest®.Vitek 2 ast-st03 result was sxt susceptible and disk diffusion and etest were sxt resistant.At this point, the customer stopped reporting any cotrimoxazole sensible results for s.Agalactiae.Biomérieux field application specialist (fas) repeated the described process and the results were the same.New samples will be sent to the laboratory as the patient had a third operation on (b)(6) 2023.Results are summarized below: october results : ast-p589 lot#: 3692211503: trimetoprima/sulfametoxazole mic10, s.February results: initial testing on (b)(6) 2023).Ast-st03 lot#: 5422257203: sxt mic10, s following incubation in aerobic environment (off-label use).Etest and disk diffusion results: no halo.Repeat testing (by biomérieux fas) on (b)(6) 2023).Ast-st03 lot#: 5422257203: sxt mic10, s following incubation in aerobic environment (off-label use).Disk diffusion results: resistant.Biomérieux global customer service (gcs) notified the customer that the recommended incubation atmosphere for the ast-st03 card testing per the eifu is 5-10% co2.The customers incubation in an aerobic environment when using vitek 2 ast-st03 test kit 20 cards is off-label use.An investigation has been initiated.
 
Manufacturer Narrative
Context: ********** a customer in spain who encountered false susceptible trimethoprim/sulfamethoxazole (sxt) results when testing multiple isolates of 1 patient strain of streptococcus agalactiae.The strain was tested using ast-p589 lot# 3692211503 and ast-st03 lot# 5422257203.On october, customer analyzed a first sample (swab from the wound) with vitek 2 (ast-p589 test kit 20 cards - 22279), which reported positive for s.Agalactiae and sensitive for sxt.She begins to be treated with this antibiotic but the infection does not resolve.Between october and february, samples from this patient continue to arrive at the laboratory, including tissue from (2) two interventions that she had to undergo for the infection (they had to remove part of her finger).All reported positive for s.Agalactiae and sensitive for sxt (methods used are unknown).Finally, in february, since the patient did not evolve favorably with the treatment, they did in parallel a test with ast-st03 card (results documented in related complaint (b)(4)) , a diffusion disk and etest.Vitek 2 ast result was sensitive and disk diffusion and etest were resistant.** batch history record and complaint trend analysis** there is no capa related to the customer¿s complaint recorded.A complaint history review was completed for this issue concluded with no implication of a trend.This complaint has not been identified as a systemic quality issue.Investigation: *************** **investigation results** the submitted strain was subcultured on cba (cos bmx) medium under co2 for ast-st03 and under aerobic atmosphere for ast-p589 and the identification to streptococcus agalactiae was confirmed on vitek 2 gp cards.The broth micro dilution (bmd) which was the reference method used for trimethoprim/sulfamethoxazole development on ast-st03 card was performed and gave: sxt ref mic > 160 mg/l (> 8/152) r on vitek 2 (aes parameters: copy of global european based + phenotypic), the testing including ast-st03 cards from the customer lot (cl: (b)(4)) and from a random lot (rl: (b)(4)) was performed and gave: sxt vitek 2 mic = 10 mg/l (= 0.5/9.5) s on both lots tested.The vitek 2 sxt mics (= 10 mg/l (= 0.5/9.5) s) are essential agreement errors compared to the reference mic (sxt ref mic > 160 mg/l (> 8/152) r) leading to very major errors of category.The agar dilution (ad) which was the method used for trimethoprim/sulfamethoxazole development on ast-p589 card was performed and gave : sxt ref mic > 640 mg/l (> 32/608) r on vitek 2 (aes parameters: eucast + phenotypic), the testing including ast-p589 cards from the customer lot (cl: (b)(4)) and from a random lot (rl: (b)(4)) was performed and gave: sxt vitek 2 mic = 10 mg/l (= 0.5/9.5) s on both lots tested.The vitek 2 sxt mics (= 10 mg/l (= 0.5/9.5) s) are essential agreement errors compared to the reference mic (sxt ref mic > 640 mg/l (> 32/608) r) leading to very major errors of category.Conclusion: ************ the false susceptible trimethoprim/sulfamethoxazole / streptococcus agalactiae customer¿s results are reproduced in-house with both incriminated cards (ast-st03 and ast-p589).The sxt vitek 2 mics are essential agreements errors compared to the respectively reference mics leading to very major errors of category.The strain presents an unusual growth pattern within the vitek 2 environment.The isolate will be added to the r&d stock collection pending customer approval.Ast-st03, lots (b)(4) (cl) and (b)(4) (rl) met final qc release criteria.The lots passed qc performance testing.
 
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Brand Name
AST-ST03 TEST KIT 20 CARDS
Type of Device
AST-ST03 TEST KIT 20 CARDS
Manufacturer (Section D)
BIOMERIEUX INC.
595 anglum road
hazelwood MO
Manufacturer (Section G)
BIOMERIEUX INC.
595 anglum road
hazelwood MO 63042
Manufacturer Contact
céline lacroix gimon
5 rue des aqueducs
craponne 69290
FR   69290
MDR Report Key16520862
MDR Text Key311571406
Report Number1950204-2023-00002
Device Sequence Number1
Product Code LON
Combination Product (y/n)N
Reporter Country CodeSP
PMA/PMN Number
K113305
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Foreign,Health Professional,User Facility
Reporter Occupation Other Health Care Professional
Type of Report Initial,Followup
Report Date 03/10/2023
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received03/10/2023
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Health Professional
Device Expiration Date01/31/2024
Device Catalogue Number421040
Device Lot Number5422257203
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Date Manufacturer Received09/28/2023
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial
Patient Sequence Number1
Patient Age32 YR
Patient SexFemale
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