FDA Medical Devices
All recall actions attributed to FDA Medical Devices in our federal database. Each record links back to the agency's official notice so you can verify status, remedy, and amendments before acting.
U.S. Food and Drug Administration — Medical device recalls
39,096 recalls · Page 199 of 782
FDA Medical Devices Recall Insight
PlainRecalls tracks 39,096 recall actions attributed to the FDA Medical Devices in our federal recall index. Across the full PlainRecalls database of 100,165 records spanning 1995 through the present, FDA Medical Devices accounts for roughly 39.0% of all indexed recalls. The agency's stated scope — U.S. Food and Drug Administration — Medical device recalls — determines what classes of products flow through its recall pipeline and how quickly notices reach consumers. With 782 pages of records at 50 recalls per page, this archive represents one of the longest continuous federal enforcement histories accessible to the public.
Looking at the 50 records on this page alone, the severity distribution skews toward 0 critical (Class I-equivalent) actions, 50 moderate recalls, and 0 lower-severity notices. Approximately 50 of 50 entries name a specific recalling firm, while 50 disclose a unit count — the gap reflects regulatory filing norms where firms disclose lot numbers or distribution channels instead of absolute quantities. This page spans recalls from Jan 11, 2023 to Jan 11, 2023, covering 7 distinct firms. Severity mix is a leading indicator: a page weighted toward critical classifications usually signals an active public-health concern, while lower-severity clusters often represent labeling, undeclared-allergen, or minor design corrections.
Agency-level browsing is useful when a defect pattern crosses categories — for example, a supplier contamination can trigger dozens of downstream recalls that share no obvious product tag but a single issuing agency. Use the pagination below to scan the full archive, or combine this agency filter with category and manufacturer views elsewhere on PlainRecalls to intersect the data. Recall records are sourced directly from FDA Medical Devices's public enforcement feeds and are updated as the agency publishes new notices; the federal record is the authoritative version, and this page aggregates what the agency itself has released. For high-stakes decisions — medical, automotive, or childcare — always click through to the recall detail page and cross-verify the recall number against the agency's current site. Record counts reflect all indexed actions regardless of status (ongoing, terminated, or completed).
PPM INDUSTRY COMBOURG CHROMID CARBA US 20 PLT, CATALOG 414012
Biomerieux Inc
Various Custom Surgical Instrument Disposable Kits: Part Numbers / Product Description 26000004M Custom Lasik Kit AMS10411A Nasal Endoscopy Pack …
Windstone Medical Packaging, Inc.
VITEK 2 REAGENT AST-GN80 TEST KIT 20 CARDS, CATALOG 413437
Biomerieux Inc
ETEST CLINICAL AMIKACIN AK 256 US S30, CATALOG 412218
Biomerieux Inc
ETEST CLINICAL RIFAMPICIN RI 32 US S30, CATALOG 412449
Biomerieux Inc
VITEK 2 REAGENT AST-N801 TEST KIT 20 CARDS, CATALOG 423416
Biomerieux Inc
BIOBALL B.SPIZIZENII NCTC 10400 550X20, CATALOG 56012
Biomerieux Inc
ETEST CLINICAL MEROPENEM MP 32 US S30, CATALOG 412401
Biomerieux Inc
ETEST CLINICAL ERAVACYCLINE ERV US S30, CATALOG 421553
Biomerieux Inc
ETEST CLINICAL COLISTIN CO 256 US B100, CATALOG 537348
Biomerieux Inc
ETEST CLINICAL ETEST MEROPENEM/VABORBACTAM MEV US S30, CATALOG 421560
Biomerieux Inc
VIDAS CLINICAL VIDAS RUB IGG 60 TESTS, CATALOG 30226
Biomerieux Inc
PPM CLINICAL CRAPONNE CHROMID VRE 20 PLT US, CATALOG 43851
Biomerieux Inc
API LISTERIA 10 STRIPS+10 MEDIA, CATALOG 10300
Biomerieux Inc
VITEK 2 REAGENT NH TEST KIT VTK2 20 CARDS, CATALOG 21346
Biomerieux Inc
VITEK 2 REAGENT AST-XN09 TEST KIT 20 CARDS, CATALOG 423425
Biomerieux Inc
VITEK MS CLINICAL REAGENT VITEK MS-DS, CATALOG 410893
Biomerieux Inc
ActiveAid 922, Shower/Commode Chair
Altimate Medical, Inc.
VITEK 2 REAGENT AST-GP78 TEST KIT 20 CARDS, CATALOG 421051
Biomerieux Inc
PPM LOMBARD PRODUCTS IRR COUNT-TACT 3P AGAR 100 PLT, CATALOG 418049
Biomerieux Inc
ETEST CLINICAL ETEST MEROPENEM MP M100 US, CATALOG 423786
Biomerieux Inc
PPM CLINICAL CHROMID MRSA 20 PLT US, CATALOG 43841
Biomerieux Inc
ETEST CLINICAL CEFTAZIDIM/AVIBACTAM US S30, CATALOG 419046
Biomerieux Inc
VITEK 2 REAGENT AST-GN79 TEST KIT 20 CARDS, CATALOG 413436
Biomerieux Inc
ETEST CLINICAL MINOCYCLINE MC 256 US S30, CATALOG 412407
Biomerieux Inc
VIDAS CLINICAL VIDAS SALMONELLA 60T, CATALOG 30702
Biomerieux Inc
PPM LOMBARD PRODUCTS TSA 3P W NEUTRALIZERS 100 PLT, CATALOG 423723
Biomerieux Inc
TEMPO REAGENTS TEMPO CONTROL KIT , CATALOG 80000
Biomerieux Inc
API 20 C AUX 25 STRIPS+25 MEDIA, CATALOG 20210
Biomerieux Inc
Programmable Diagnostic Computer
Siemens Medical Solutions USA, Inc
VITEK 2 REAGENT AST-GN81 TEST KIT 20 CARDS, CATALOG 413438
Biomerieux Inc
VITEK 2 REAGENT AST-GP75 TEST KIT 20 CARDS, CATALOG 415670
Biomerieux Inc
PPM LOMBARD PRODUCTS TSA 3P W NEUTRALIZERS 100 PLT, CATALOG 419014
Biomerieux Inc
PPM CLINICAL CRAPONNE CLINICAL CHROMID CANDIDA 20 PLATES, CATALOG 43631
Biomerieux Inc
PPM LOMBARD PRODUCTS CT&TI-TSA + L & P80 10PLT, CATALOG C6045-TI
Biomerieux Inc
GENE-UP REAGENT GENE-UP Salmonella 2, CATALOG 423105
Biomerieux Inc
Liquid Assayed Specific Protein Control Level 2- In vitro diagnostic use, in the quality control of serum on clinical chemistry and immunoassay syst…
Randox Laboratories Ltd.
ETEST CLINICAL CEFTRIAXONE TX 32 US S30, CATALOG 412302
Biomerieux Inc
PPM LOMBARD PRODUCTS R2A MEDIUM 10PLT, CATALOG M1065
Biomerieux Inc
VIDAS CLINICAL QCV-QUALITY CONTROL VIDAS 60T, CATALOG 30706
Biomerieux Inc
VERIFY Steam Test Pack (20 Tests and 20 controls) Item Number: S3069 Intended for use in installation testing and routine monitoring of steam and…
Steris Corporation
PPM INDUSTRY COMBOURG LPT BROTH (4X3L), CATALOG 410849
Biomerieux Inc
PPM CLINICAL CHROMID MRSA S AUREUS 20PLT US, CATALOG 414524
Biomerieux Inc
GENE-UP REAGENT GENE-UP LYSIS KIT, CATALOG 414057
Biomerieux Inc
ETEST CLINICAL IMIPENEM IP 32 US S30, CATALOG 412373
Biomerieux Inc
PREVI COLOR GRAM REAGENT NOZZLE CLEANING SOLUTION (NA), CATALOG 29588
Biomerieux Inc
Beaver EdgeAhead Stiletto/MVR Knife .90mm Straight (20G)-for ocular paracentesis incisions in cataract procedures. Part Number: 376630
Beaver Visitec International, Inc.
VITEK 2 REAGENT AST-ST02 TEST KIT 20 CARDS, CATALOG 420915
Biomerieux Inc
VITEK 2 REAGENT AST-GN99 TEST KIT 20 CARDS, CATALOG 423102
Biomerieux Inc
API NIT1 NIT2 REAGENTS, CATALOG 70442
Biomerieux Inc
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Disclaimer: This information is provided for informational purposes only and does not constitute professional advice. Consult a qualified professional before making decisions based on this data.
- Source: FDA Medical Devices — verify with the issuing agency: official recall page →
- Source: PlainRecalls Data Index — aggregated from FDA openFDA, CPSC, and NHTSA public databases
Read our methodology — how this data is sourced, computed, and verified.