PlainRecalls

2017 Recall Year Insight

Federal agencies issued 7,681 product recalls indexed by PlainRecalls in calendar year 2017. That represents about 7.36% of the 104,423 total recalls we track from 1995 through the present, and averages roughly 21.0 recalls per day across the FDA, CPSC, USDA FSIS, 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 154 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 1 critical, 48 moderate, and 1 lower-severity recalls. The page references 9 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, USDA FSIS, 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

IMRI MOTOR Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Foot Control, SC2100 Product Usage: Electric system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Accu-Chek Connect Diabetes Management App versions 2.0.0, 2.0.1 and 2.1.0 for iOS and Android Product Usage: This is a digital product available for download direct to customers from the Apple App Store and the Google Play Store. The total number of downloads is not available. The number of unique users for each affected version from the date of initial distribution through 03/23/2017 is noted in 7a. However, some users will have used all three affected versions as they upgraded from version

Roche Diabetes Care, Inc.

FDA Devices Moderate May 10, 2017

22CM MICRO REVISION ATTACH, BLACK MAX

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Autolube-III with NK Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

RENOVATION, THIN OSTEOTOME BLADE, 8 MM X 5 INCH, REF 71369408, STERILE R, QTY: (1)

Smith & Nephew, Inc.

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

AQUIOS CL Flow Cytometer, Ref no. B30166, Software Versions 2.0 and 2.0.1 Product Usage: The AQUIOS CL Flow Cytometer is intended for use with in vitro diagnostic flow cytometric applications using up to four fluorescent detection channels using a blue (488 nm) laser, two light scatter detection channels and electronic volume (EV).

Beckman Coulter Inc.

FDA Devices Low May 10, 2017

The TM Ardis Interbody System implant is a convex, straight TLIF or PLIF device for interbody fusion of the anterior column of the spine. TM Ardis is designed for fusing the adjacent bony surfaces and may be used to replace a disc at one or two contiguous levels in L2-S1. The superior and inferior surfaces of the device are textured to provide increased stability and convex to conform to the vertebral endplates. The device also has two slots on the posterior end to mate with the insertion instru

Zimmer Trabecular Metal Technology, Inc.

FDA Devices Moderate May 10, 2017

AL-III W/ male disconnect and 30ft hose Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

RENOVATION, THIN OSTEOTOME BLADE, 10 MM X 3 INCH, REF 71369210, STERILE R, QTY: (1)

Smith & Nephew, Inc.

FDA Devices Moderate May 10, 2017

RENOVATION, THIN OSTEOTOME BLADE, 10 MM X 3 INCH, REF 71369410, STERILE R, QTY: (1)

Smith & Nephew, Inc.

FDA Devices Moderate May 10, 2017

Adult Craniotome Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

RENOVATION, THIN OSTEOTOME BLADE, 12 MM X 3 INCH, REF 71369212, STERILE R, QTY: (1)

Smith & Nephew, Inc.

FDA Devices Moderate May 10, 2017

RENOVATION, THIN OSTEOTOME BLADE, 20 MM X 3 INCH, REF 71369220, STERILE R, QTY: (1)

Smith & Nephew, Inc.

FDA Devices Moderate May 10, 2017

20.2cm Heavy Duty Long Heavy Short Attachment

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

5.0cm Heavy Duty Short Attachment

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Sagittal MICRO-SAW

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

XMAX Motor (Pneumatic Drill System) Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Pediatric Craniotome

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

14cm QD Angle Attachment

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

If Hip, Sterile Polar Dressing P/N 10680 Product Usage: These products are sterile dressings used as an insulation barrier between the Polar Care cold therapy pad and the skin. Sterile dressings are typically applied in a non-sterile environment after post-op and on occasion may be applied in a sterile environment. Breg has determined that a small percentage (approximately 0.22%) of these products may have been sent with unsealed pouches by the contract manufacturer. Customers will be contac

Breg Inc

FDA Devices Moderate May 10, 2017

Dale Medical Stabilock Endotracheal Adhesive Base Product # 273 The Dale Stabilock Endotracheal Tube Bolder 270 is a 2 piece device consisting of an adhesive base, Dale product number 273, that attaches to the patient's skin and a cushioned neckband with tube channel that attaches with hook & loop closures. The 270 is used to secure and stabilize endotracheal tubes, preventing unnecessary movement which can help prevent accidental .extubation

Dale Medical Products, Inc.

FDA Devices Moderate May 10, 2017

Oscillating MICRO-SAW Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

8.2CM ATTACHMENT, BLACK MAX Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

16.5CM MICRO REVISION ATTACH, BLACK MAX

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

LARGE CRANIOTOME, BLACK MAX

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

KEYLESS DRIVER, BLACK MAX

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

10.5CM ANGLE ATTACHMENT, BLACK MAX

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

11.25CM ATTACHMENT, BLACK MAX

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

8CM ANGLE ATTACHMENT, BLACK MAX

The Anspach Effort, Inc.

FDA Devices Critical May 10, 2017

Newport Medical HT70 and HT70- Plus Ventilators, Rx Only Product Usage: The Newport HT70 family of ventilators is intended to provide continuous or intermittent positive pressure mechanical ventilatory support for the care of individuals who require mechanical ventilation through invasive or non-invasive interfaces. Specifically, the Newport HT70 family of ventilators is applicable for infant, pediatric and adult patients greater than or equal to 5 kg (11 lbs). The Newport HT70 is a restrict

Newport Medical Instruments Inc

FDA Devices Moderate May 10, 2017

7.2cm Adjustable Drill Guide Product Usage: Electric system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

B-SAGITTAL ASSEMBLY Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Minimal Access Straight Driver Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

SMALL ATTACHMENT, JACOBS CHUCK

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Chuck Driver System

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Olympus ENDOEYE HD II Video Telescopes Models: WA50040A Endoeye HD II, 10 mm, 0 deg., autoclavable; WA50042A Endoeye HD II, 10 mm, 30 deg., autoclavable; repair cable 10mm 0/30 deg., part number W7100603

Olympus Corporation of the Americas

FDA Devices Moderate May 10, 2017

Console, eMax2 Plus Product Usage: Electric system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

RENOVATION, RADIAL OSTEOTOME BLADE, SIZE 12, REF 71369312, STERILE R, QTY: (1)

Smith & Nephew, Inc.

FDA Devices Moderate May 10, 2017

RENOVATION, ROUNDED END, THIN OSTEOTOME BLADE, 20 MM, REF 71369420, STERILE R, QTY: (1)

Smith & Nephew, Inc.

FDA Devices Moderate May 10, 2017

19CM ATTACHMENT, BLACK MAX

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Sagittal Saw Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Minimal Access Attachment, BLACK MAX Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Minimal Access Attachment Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

16cm Minimally Invasive Attachment Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Bearing Sleeve, 15CM Straight Taper Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

6.5CM ADLT CRANI, THIN FT PLATE Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

Otologic Curved Micro Product Usage: Pneumatic system

The Anspach Effort, Inc.

FDA Devices Moderate May 10, 2017

8.0cm Medium Attachment Product Usage: Pneumatic system

The Anspach Effort, 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: USDA FSIS Recalls - calendar-year meat, poultry, and processed egg product recall filings
  • Source: CPSC + NHTSA - consumer product and vehicle recall feeds for 2017

Every figure on PlainRecalls is rendered directly from official FDA, CPSC, USDA FSIS and NHTSA recall records; no number is typed in by an editor. Figures cover calendar year 2017 across the FDA, CPSC, USDA FSIS 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 September 2026.