PlainRecalls

Aniara Diagnostica LLC

Compiled from official public sources by the publisher.

11 recalls on record · Latest: Aug 12, 2026

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Agency notice ledger

Federal filing book Aniara Diagnostica LLC LIGHT-BOOK · SINGLE-AGENCY

#1,315 of 14,151 · 11 notices · 0.011% archive

  • BOOK 11 notices
  • RANK #1,315 of 14,151
  • SHARE 0.011% archive
  • AGENCY FDA Devices (11)
  • CAT medical devices
  • CATS 1 category
  • LATEST Aug 12, 2026
  • PHOTO Agfa Corp.

Nearest notice-volume peer: Agfa Corp. (0 notice gap)

Aniara Diagnostica LLC accounts for about 0.011% of the 104,423-notice archive on 11 distinct filings — a mid share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Where Aniara Diagnostica LLC sits among 14,151 recalling firms

Aniara Diagnostica LLC ranks 1,315th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Aniara Diagnostica LLC vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

11 1315th of 14151 higher than 12,735 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13

Aniara Diagnostica LLC in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Aniara Diagnostica LLC holds about 0.011% of archive notices alongside 11 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Aug 12, 2026

5-PLASMA Bivalirudin AMR Verification Kit, Model Number 5D-45905
FDA Devices Moderate Aug 12, 2026

5-PLASMA Bivalirudin Calibrator, Model Number 5D-46905
FDA Devices Moderate Aug 12, 2026

5-PLASMA Bivalirudin Control, Model Number 5D-44905
FDA Devices Moderate May 20, 2026

ZYMUTEST HIA IgG, in vitro diagnostic ELISA kit, Ref. RK040A
FDA Devices Moderate Mar 15, 2023

BIOPHEN Protein C 5 kit is for in vitro quantitative determination of Protein C activity on human citrated plasma. Protein C is a glycoprotein, vitamin K dependent, which inhibits coagulation. Protein C in plasma is measured following a specific activation with Protac (Agkistrodom Contortrix), an enzyme extracted from snake venom. Activated protein C hydrolysis the chromogenic substrate (SaPC-21) which release para-nitroaniline (pNA). The amount of pNA released (measured by absorbance at 405 nm)
FDA Devices Low Sep 21, 2022

BIOPHEN UFH Control Plasma
FDA Devices Moderate Aug 28, 2019

ZYMUTEST HIA MonoStrip, IgG ELISA kit, Model No. RK041A, for in vitro diagnostic use.
FDA Devices Moderate Aug 28, 2019

ZYMUTEST HIA MonoStrip, IgGAM ELISA kit, Model No. RK041D, for in vitro diagnostic use.
FDA Devices Low Apr 24, 2019

BIOPHEN UFH Control C1, REF 224101
FDA Devices Low Apr 24, 2019

BIOPHEN LMWH Control C4, REF 224201
FDA Devices Low Apr 24, 2019

BIOPHEN UFH Control C2, REF 223901

Aniara Diagnostica LLC holds a measurable archive slice

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar recall count

Nearest multi-notice firms by distinct-event totals (11 here — thin-book).

Agfa Corp. 11 Ajinomoto Foods North America Inc. 11 Akron Pharma, Inc. 11 Amendia, Inc 11 Arg Laboratories, Inc. 11

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

Agfa Corp. 11 Amendia, Inc 11 Arjohuntleigh Polska Sp. z.o.o. 11 Caire, Inc. 11

Frequently Asked Questions

How many federal recall notices name Aniara Diagnostica LLC? ▼
PlainRecalls indexes 11 distinct federal recall events naming Aniara Diagnostica LLC, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Aniara Diagnostica LLC sit among other recalling firms? ▼
Aniara Diagnostica LLC ranks #1,315 of 14,151 by distinct recall-event count among 14,151 firms in this archive (90th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Aniara Diagnostica LLC's notices? ▼
FDA Devices accounts for 11 of this firm's 11 indexed notices.
What product category dominates Aniara Diagnostica LLC's filing book? ▼
Filings for Aniara Diagnostica LLC span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Aniara Diagnostica LLC: 11 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Aniara Diagnostica LLC; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026