PlainRecalls

2017 Recalls

6,356 recalls · Page 61 of 128

2017 Recall Year Insight

Federal agencies issued 6,356 product recalls indexed by PlainRecalls in calendar year 2017. That represents about 7.57% of the 83,949 total recalls we track from 1995 through the present, and averages roughly 17.4 recalls per day across the FDA, CPSC, NHTSA, and USDA FSIS 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 128 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, NHTSA, or USDA FSIS 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-N245), REF 413394, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-GN72), REF 413403, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N357), IVD, REF 421451, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK 2 Anaerobic and Corynebacteria identification card (ANC), REF 21347, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-GN92), IVD, REF 414963, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

1) Pressure Injectable ARROW(R) PICC Kit with Chlorag+ard(R) Technology The Pressure Injectable PICC with Chlorag+ard Antimicrobial and Antithrombog…

Arrow International Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Positive Susceptibility card (AST-P642), IVD, REF 418604, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

Sutures. ENDO STITCH: ENDO STITCH POLYSORB 0 48" U/D DLU SU, Item Number: 170056; ENDO STITCH POLYSORB 0 48" VIO DLU SU, Item Number: 170052; ENDO S…

Medtronic

FDA Devices Moderate Jun 21, 2017

Best Practice Kit, Item Numbers: 00Z2064, 00Z2150, 00Z2190, 00Z2192, 00Z2211, 00Z2212, 00Z2216, 00Z2217, 00Z2312

Medtronic

FDA Devices Moderate Jun 21, 2017

GE Healthcare Discovery NM/CT 570c X-ray system

GE Healthcare, LLC

FDA Devices Moderate Jun 21, 2017

USPACK-SUTURE KIT; Item Number: US1672

Medtronic

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N334), IVD, REF 418984, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N314), IVD, REF 417027, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N264), REF 413864, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N263), REF 413755, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N228), REF 413145, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N249), REF 413572, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

Merge PACS software. Merge PACS (Picture Archiving Communication System) is designed and marketed for soft copy reading, communication, and storage…

Merge Healthcare, Inc.

FDA Devices Moderate Jun 21, 2017

1) Pressure Injectable Multi-Lumen Central Venous Catheterization Kit 2) Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blu…

Arrow International Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Positive Susceptibility card (AST-P597), REF 22298, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-GN49), REF 412091, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

Xl por st 25.5x220mm, bowed\, bowed, 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-N253), REF 413722, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

GE Healthcare Discovery NM/CT 670. 670 Pro, 670 ES X-ray system

GE Healthcare, LLC

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N202), REF 412863, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-GN77), REF 413434, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-GN65), REF 412608, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

Fem IM Nail 16mmdx44cm, Sterile, Rod, fixation, intramedullary and accessories- Specific Knee, Hip and Nail Implants

Zimmer Biomet, Inc.

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Positive Susceptibility card (AST-P608), REF 22336, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-XN05), REF 413230, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

Sutures. MAXON: MAXON 4/0 5X18" GREEN CV-24 D-TACH; Item Number: 8886621933; MAXON 5/0 5X18 GR CV-23 D-TACH; Item Number: XX2109; MAXON* 4/0 5X30 GR…

Medtronic

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Positive Susceptibility card (AST-P633), REF 414994, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

Fem IM Nail 16mmdx42cm, 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-N231), REF 413115, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

Pointe Scientific Hitachi Total Bilirubin Rl Reagent Product Usage: Two part Chemistry Reagent Hitachi Total Bilirubin Rl Reagent is used with Hi…

Medtest Holdings, Inc.

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N355), IVD, REF 421351, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

GE Healthcare Discovery Ml DR X-ray system

GE Healthcare, LLC

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Positive Susceptibility card (AST-P632), REF 415059, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

GE Healthcare Optima CT540 X-ray system

GE Healthcare, LLC

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N254), REF 413723, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-GN90), REF 414779, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK 2 Gram Negative Susceptibility card (AST-N102), REF 22258, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Positive Susceptibility card (AST-P612), REF 22359, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter and Sharps Safety Features. The multiple-lumen…

Arrow International Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N270), REF 414162, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

Single-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Catheter, Catheter, Percutaneous The Arrow Single-Lumen Catheter permits venous…

Arrow International Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N317), IVD, REF 417558, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N275), REF 414313, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

VITEK¿ 2 Gram Negative Susceptibility card (AST-N303), IVD, REF 416590, 20 cards per carton.

Biomerieux Inc

FDA Devices Moderate Jun 21, 2017

Sutures. POLYSORB: POLSORB 0 18 U/D PRECUT 126R, Item Number: L4; POLSORB 0 18 VIO PRECUT 226T; Item Number: L14; POLSORB 0 30 VIO PRECUT 227C, Item…

Medtronic

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 + USDA FSIS — consumer product, vehicle, and meat/poultry recall feeds for 2017