PlainRecalls

2017 Recalls

6,356 recalls · Page 76 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, 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 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 48 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 May 10, 2017

90 degree Contra Angle Attachment Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Foot control irrigation system Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

19cm Attachment, Black Max Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Autolube-III with Foot Guard Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

11.0cm Long Attachment Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Autolube-III with Irrigation Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

5.0cm Short Attachment

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Large Craniotome Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

8cm QD Angle Attachment

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Dressing M/U XL, P/N 02344 Product Usage: These products are sterile dressings used as an insulation barrier between the Polar Care cold therapy …

Breg Inc

FDA Devices Moderate May 10, 2017

13.5CM ANGLE ATTACHMENT, BLACK MAX

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

26.65CM ATTACHMENT, BLACK MAX

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Bearing Sleeve, 10CM Straight Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Autolube-III with 20ft hose Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

eMax2 PLUS Product Usage: Electric system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Reciprocating MICRO SAW

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Second generation neoBLUE LED Phototherapy Light (neoBLUE 2) sold between 2003 and 2008. Catalog Part Number 010066. Top Assembly Part Numbers: 0409…

Natus Medical Incorporated

FDA Devices Moderate May 10, 2017

Electronic Foot Control with Direction or Irrigation Switches Product Usage: Electric system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Compact Speed Reducer, 60:1

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Dressing, Knee L/XL, P/N 04708 Product Usage: These products are sterile dressings used as an insulation barrier between the Polar Care cold ther…

Breg Inc

FDA Devices Moderate May 10, 2017

6.1CM ATTACHMENT, BLACK MAX Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

7.5cm QD Angle Attachment

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

10.5cm Long Attachment, Non-Tapered End Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Destination Renal Guiding Sheath Intended for the introduction of interventional and diagnostic devices into the human vasculature.

Terumo Medical Corporation

FDA Devices Moderate May 10, 2017

10.5cm Long Attachment Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

9.4CM MICRO REVISION ATTACH, BLACK MAX

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

CONTRA ANGLE ATTACHMENT, BLACK MAX

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

ADJUSTABLE DRILL GUIDE, BLACK MAX

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Bearing Sleeve, 19CM Straight Taper Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

8.0CM Heavy Duty Medium Attachment Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Dressing Back, P/N 09810 Product Usage: These products are sterile dressings used as an insulation barrier between the Polar Care cold therapy pa…

Breg Inc

FDA Devices Moderate May 10, 2017

Sonesta S2; Article numbers: 525-S2-110V and 525¿¿S2-220V

Sonesta Medical Ab

FDA Devices Moderate May 10, 2017

GREEN ROTATING CRANIOTOME, BLACK MAX

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

7.5CM ANGLE ATTACHMENT, BLACK MAX

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

SurFlo IV Catheter

Terumo Medical Corporation

FDA Devices Moderate May 10, 2017

14CM ANGLE ATTACHMENT, BLACK MAX

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Dressing Knee/Shldr, P/N 02328 Product Usage: These products are sterile dressings used as an insulation barrier between the Polar Care cold ther…

Breg Inc

FDA Devices Moderate May 10, 2017

System Console, Single Port, no irrigation

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

12.4cm Heavy Duty Long Heavy Short Attachment Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

RENOVATION, RADIAL OSTEOTOME BLADE, SIZE 16, REF 71369316, STERILE R, QTY: (1)

Smith & Nephew, Inc.

FDA Devices Moderate May 10, 2017

45 degree Contra Angle Attachment Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

90 DEG RIGHT ANGLE ATTACH, BLACK MAX

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Bearing Sleeve, 15CM Curved Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

The JETSTREAM is a rotational atherectomy catheter system designed for use in debulking and treating vascular disease in the peripheral vasculature. …

Boston Scientific Corporation

FDA Devices Moderate May 10, 2017

IMRI CRANI-A ATTACHMENT Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

RENOVATION, RADIAL OSTEOTOME BLADE, SIZE 10, REF 71369310, STERILE R, QTY: (1)

Smith & Nephew, Inc.

FDA Devices Moderate May 10, 2017

eMax2 Motor Assembly Product Usage: Electric system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

16CM MIN INVASIVE ATTACH, BLACK MAX

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

AL-III-DISS Adapter Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Dressing Shldr, P/N 04908 Product Usage: These products are sterile dressings used as an insulation barrier between the Polar Care cold therapy p…

Breg 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