PlainRecalls

2017 Recalls

7,536 recalls · Page 73 of 151

2017 Recall Year Insight

Federal agencies issued 7,536 product recalls indexed by PlainRecalls in calendar year 2017. That represents about 7.41% of the 101,704 total recalls we track from 1995 through the present, and averages roughly 20.6 recalls per day across the FDA, CPSC, and NHTSA combined. Year-level views are the cleanest way to see macro patterns: volume spikes often correlate with new regulatory priorities (e.g., infant-sleep products after 2021, lithium-ion batteries after 2022), supply-chain contamination events, or changes in agency enforcement intensity, while quiet years can reflect either genuine product-safety improvements or reduced agency staffing and reporting lag. With 151 pages at 50 recalls each, browsing this year end-to-end gives a statistically representative sample of what the federal recall pipeline looked like in 2017.

On this page of 50 records, severity classification shows 0 critical, 50 moderate, and 0 lower-severity recalls. The page references 7 distinct recalling firms operating in 1 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (50), which matters because each agency's recall authority, hazard framing, and remedy mechanism differ, an FDA food recall, a CPSC consumer-product recall, and a NHTSA vehicle recall are legally distinct instruments even when the underlying hazard language sounds similar. Reviewing the dominant agency for a given year is one of the fastest ways to understand where federal attention was concentrated.

Year-indexed browsing serves three practical purposes: historical research (tracking how a hazard class evolved over time), consumer action (finding whether a product purchased in 2017 was later recalled), and journalistic or regulatory context (understanding what the enforcement landscape looked like in a given period). Every record on this page links to a full detail view with the hazard, remedy, distribution, and agency-assigned recall number, always use that recall number to verify current status directly with the issuing agency before acting on time-sensitive remedies, because agencies amend, terminate, and expand recalls in the months and years after initial publication. Data on this page reflects federal agency public filings; the agency's live record remains authoritative for legal, medical, or safety decisions. Verify with FDA openFDA, CPSC, or NHTSA for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N364), IVD, REF 421693, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Fungal Susceptibility card (AST-YS08), IVD, REF 420739, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N227), REF 413144, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-P625), REF 413727, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Positive Susceptibility card (AST-P641), IVD, REF 418590, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Positive Susceptibility card (AST-GP68), REF 22231, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-XN06), REF 413944, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N201), REF 412862, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

Video Bronchoscope

Pentax of America Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N193), REF 412604, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

Por fullct fem st 20x200mm, Sterile, Rod, fixation, intramedullary and accessories- Specific Knee, Hip and Nail Implants

Zimmer Biomet, Inc.

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N328), IVD, REF 418630, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

GE Healthcare Lightspeed RT16 X-ray system

GE Healthcare, LLC

FDA Devices Moderate Jun 21, 2017

Arrow Multi-Lumen CVC Kit The Arrow Two-Lumen Central Venous Access device permits venous access and catheter introduction to the central circulatio…

Arrow International Inc

FDA Devices Moderate Jun 21, 2017

Segmental fluted stem, 19x250mm bwd, Sterile, Rod, fixation, intramedullary and accessories- Specific Knee, Hip and Nail Implants

Zimmer Biomet, Inc.

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-GN84), REF 413410, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

GE Healthcare Discovery Ml X-ray system

GE Healthcare, LLC

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N243), REF 413392, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Positive Susceptibility card (AST-P638), IVD, REF 418423, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

Segmental malefemale taper, 200mm, Sterile, Rod, fixation, intramedullary and accessories- Specific Knee, Hip and Nail Implants

Zimmer Biomet, Inc.

FDA Devices Moderate Jun 21, 2017

Fem IM Nail 15mmdx44cm, Sterile, Rod, fixation, intramedullary and accessories- Specific Knee, Hip and Nail Implants

Zimmer Biomet, Inc.

FDA Devices Moderate Jun 21, 2017

GE Healthcare Discovery NM/CT 670 CZT X-ray system

GE Healthcare, LLC

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-GN93), REF 414985, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK 2 Gram-Positive identification card (GP), IVD, REF 21342, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N213), REF 413063, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

Vue Optic Visualization Source, Flexor Vue Deflecting Endoscopic System, Endoscope, Fiber Optic, Supplied sterilized by ethylene oxide gas in peel-op…

Cook Inc.

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-GN73), REF 413404, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N271), REF 414163, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N237), REF 413172, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Fungal Susceptibility card (AST-YS01), REF 22108, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

GE Healthcare Optima CT660, CT680 X-ray system

GE Healthcare, LLC

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N215), REF 413065, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram-Negative identification card (GN), IVD, REF 21341, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-GN75), REF 413432, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

Por fullct fem st 20x200mm, Sterile, Rod, fixation, intramedullary and accessories- Specific Knee, Hip and Nail Implants

Zimmer Biomet, Inc.

FDA Devices Moderate Jun 21, 2017

CADD¿ High Volume Administration Set with FlowStop, 21-7381-24. Product Usage: The CADD¿ High-Volume Administration set is designed for use with…

Smiths Medical ASD Inc.

FDA Devices Moderate Jun 21, 2017

4.5 BROAD SCP PLT 26-H STER

Zimmer Biomet, Inc.

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N208), IVD, REF 413062, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N238), REF 413203, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N204), REF 412865, 20 cards per carton. .

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-GN81), REF 413438, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

ARROWg+ard Blue CVC Kit The ARROWg+ard Blue CVCs are intended to permit venous access to the central circulation

Arrow International Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N209), REF 412938, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-GN87), REF 413943, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N233), REF 413117, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N320), IVD, REF 418204, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N352), IVD, REF 421258, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

Segmental vss bowed 19x190mm, Sterile, Hip joint, metal/ceramic/polymer, semi-constrained, cemented or nonporous uncemented prosthesis- Specific Kn…

Zimmer Biomet, Inc.

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Positive Susceptibility card (AST-P640), IVD, REF 418579, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

Fem IM Nail 16mmdx50cm, Sterile, Rod, fixation, intramedullary and accessories- Specific Knee, Hip and Nail Implants

Zimmer Biomet, Inc.

Nearby Recall Years

Browse recalls from adjacent calendar years to see how federal enforcement volume has shifted over time.

Compare 2017 with 2016 →

Data Sources

  • Source: FDA openFDA Enforcement API - calendar-year recall filings for food, drugs, and devices
  • Source: CPSC + NHTSA - consumer product and vehicle recall feeds for 2017

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Figures cover calendar year 2017 across the FDA, CPSC and NHTSA federal recall feeds. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of August 2026.