TGA tested 28 mRNA batches for Residual DNA & Endotoxin - Please explain

12 mins video with screensharing of websites and documents on 5.1.2025:
1. The TGA (Therapeutic Goods Administration) in Australia provided a publication on their website on 7.11.2024 entitled "Summary report of residual DNA and endotoxin on CoVID-19 mRNA vaccines conducted by TGA Laboratories". There were 28 batch numbers listed as being tested by the TGA i.e. 15 Pfizer (Comirnaty) and 13 Moderna (Spikevax).
https://www.tga.gov.au/resources/publication/tga-laboratory-testing-reports/summary-report-residual-dna-and-endotoxin-covid-19-mrna-vaccines-conducted-tga-laboratories
2. The TGA stated "The TGA Laboratories tested 28 batches of mRNA vaccines and confirmed that all batches complied with the World Health Organization recommended limit of up to 10 ng per dose."
3. The TGA also stated "Every batch of both mRNA vaccines released in Australia was tested for bacterial endotoxins using a validated Limulus amebocyte lysate (LAL) assay. Endotoxin was tested to a level of 5 Endotoxin Units (EU) per mL and all batches were below this level."
4. However, 3 of the listed 28 batch numbers (1 x Pfizer and 2 x Moderna) were NOT fully tested as documented under the TGA's own webpage "Batch release assessment of COVID-19 vaccines". Moderna batch numbers 0000036 and 0000037 were shown not tested and Pfizer LD8974 was not fully tested. Click link and use search engine to type in batch numbers and read columns across. https://www.tga.gov.au/products/covid-19/covid-19-vaccines/batch-release-assessment-covid-19-vaccines
5. 2 of the 15 Pfizer batch numbers listed on the TGA's publication 7.11.2024 - HH1297 and HJ3095, led to deaths being reported on the TGA DAEN (Database of Adverse Event Notifications) and a number of other cases reported.
6. So, how can the TGA publish their report on 7.11.2024 entitled "Summary report of residual DNA and endotoxin on CoVID-19 mRNA vaccines conducted by TGA laboratories", then list 2 Moderna untested batch numbers and 1 Pfizer not fully tested batch number and still state: "The TGA Laboratories tested 28 batches of mRNA vaccines and confirmed that all batches complied with the World Health Organization recommended limit of up to 10 nd per dose."
7. TGA only tested 28 mRNA batch numbers that were released after Jan. 2023 (Pfizer) and May 2023 (Moderna) for residual DNA and bacterial endotoxin. What about all the other mRNA batch numbers starting from Pfizer EP2163 released 9.2.2021 and the worst batch number for adverse events reported in Australia, Pfizer ER7449 released 27.2.2021 resulting in 3,835 cases including 43 reported deaths (as per FOI 5293, published 26.8.2024).

Please explain?