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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 89446

5 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
June 06, 2017
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Microbiologics Inc

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

5 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 5

Microbiologics QC Sets and Panels: Helix Elite. Extended Enteric Bacterial Verification Panel (Inactivated Pellet) includes 21 pellets each comprised of the following 8 organisms: 1. S. Typhimurium derived from NCTC 74, 2. S. sonnei derived from NCTC 12984, 3. E. coli derived from CDC 2010C-3114 (STEC), 4. C. jejuni derived from NCTC 11322, 5. P. shigelloides derived from NCTC 10363, 6. Y. enterocolitica derived from NCTC 11174, 7. E. coli derived from NCTC 11602 (ETEC), 8. V. parahaemolyticus derived from NCTC 13209

Z-0697-2022
Recall number
Z-0697-2022
Initiated
June 06, 2017
Classification
Class II
Status
Terminated
Recalling firm
Microbiologics Inc
Quantity
8 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Real-time shelf life testing failed at 24 months

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Real-time shelf life testing failed at 24 months

Code information

Catalog Number: 8191, Lot Number: 8191-01, UDI: 70845357041240

Distribution pattern

Worldwide distribution - US Nationwide distribution in the states of AK, CA, DC, FL, IA, ID, KS, LA, MD, MN, MO, NE, NH, NJ, NY, OH, OK, PA, SC, TX, VA, WA, WV and the countries of Australia, Belgium, Canada, India, United Kingdom.

device · product 2 of 5

Microbiologics QC Sets and Panels. BD MAX" CT/GC/TV Verification and Control Panel. Containing High, Medium and Low Level Controls.

Z-0698-2022
Recall number
Z-0698-2022
Initiated
June 06, 2017
Classification
Class II
Status
Terminated
Recalling firm
Microbiologics Inc
Quantity
29 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Real-time shelf life testing failed at 24 months

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Real-time shelf life testing failed at 24 months

Code information

Catalog Number: 8193; Lot Number: 8193-04, 8193-06; UDI: 70845357041080

Distribution pattern

Worldwide distribution - US Nationwide distribution in the states of AK, CA, DC, FL, IA, ID, KS, LA, MD, MN, MO, NE, NH, NJ, NY, OH, OK, PA, SC, TX, VA, WA, WV and the countries of Australia, Belgium, Canada, India, United Kingdom.

device · product 3 of 5

Helix Elite" Molecular Standards: Inactivated Standard. Inactivated Respiratory Syncytial Virus A Strain Long. Target pathogens are lyophilized in a PCR compatible matrix, and stable at 2¿C-25¿C through the expiration date. Each lyophilized pellet is packaged in a single-use foil pouch. Each kit contains 5 unassayed lyophilized pellets, packaged in individual vials for ease-of-use and to avoid cross contamination.

Z-0699-2022
Recall number
Z-0699-2022
Initiated
June 06, 2017
Classification
Class II
Status
Terminated
Recalling firm
Microbiologics Inc
Quantity
1 unit

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Real-time shelf life testing failed at 24 months

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Real-time shelf life testing failed at 24 months

Code information

Catalog Number: HE0028N; Lot Number: HE0028N-102-1; UDI: 10845357042023

Distribution pattern

Worldwide distribution - US Nationwide distribution in the states of AK, CA, DC, FL, IA, ID, KS, LA, MD, MN, MO, NE, NH, NJ, NY, OH, OK, PA, SC, TX, VA, WA, WV and the countries of Australia, Belgium, Canada, India, United Kingdom.

device · product 4 of 5

Helix Elite" Molecular Standards: Inactivated Standard. Inactivated Neisseria gonorrhoeae Strain GL0071.

Z-0700-2022
Recall number
Z-0700-2022
Initiated
June 06, 2017
Classification
Class II
Status
Terminated
Recalling firm
Microbiologics Inc
Quantity
1

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Real-time shelf life testing failed at 24 months

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Real-time shelf life testing failed at 24 months

Code information

Catalog Number: HE0041N; Lot Number: HE0041N-102-1; UDI: 10845357042153

Distribution pattern

Worldwide distribution - US Nationwide distribution in the states of AK, CA, DC, FL, IA, ID, KS, LA, MD, MN, MO, NE, NH, NJ, NY, OH, OK, PA, SC, TX, VA, WA, WV and the countries of Australia, Belgium, Canada, India, United Kingdom.

device · product 5 of 5

Helix Elite" Molecular Standards: Inactivated Standard. Inactivated Influenza A/B and Respiratory Syncytial Virus

Z-0701-2022
Recall number
Z-0701-2022
Initiated
June 06, 2017
Classification
Class II
Status
Terminated
Recalling firm
Microbiologics Inc
Quantity
1 unit

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Real-time shelf life testing failed at 24 months

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Process design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Real-time shelf life testing failed at 24 months

Code information

Catalog Number: HE0044N; Lot Number: HE0044N-103-1; UDI: 10845357042184

Distribution pattern

Worldwide distribution - US Nationwide distribution in the states of AK, CA, DC, FL, IA, ID, KS, LA, MD, MN, MO, NE, NH, NJ, NY, OH, OK, PA, SC, TX, VA, WA, WV and the countries of Australia, Belgium, Canada, India, United Kingdom.