2017 Recalls
7,480 recalls · Page 90 of 150
2017 Recall Year Insight
Federal agencies issued 7,480 product recalls indexed by PlainRecalls in calendar year 2017. That represents about 8.91% of the 83,949 total recalls we track from 1995 through the present, and averages roughly 20.5 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 150 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, 49 moderate, and 1 lower-severity recalls. The page references 12 distinct recalling firms operating in 1 distinct product categories, with 49 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.
Sonesta S2; Article numbers: 525-S2-110V and 525¿¿S2-220V
Sonesta Medical Ab
GREEN ROTATING CRANIOTOME, BLACK MAX
The Anspach Effort, Inc.
7.5CM ANGLE ATTACHMENT, BLACK MAX
The Anspach Effort, Inc.
SurFlo IV Catheter
Terumo Medical Corporation
14CM ANGLE ATTACHMENT, BLACK MAX
The Anspach Effort, Inc.
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
System Console, Single Port, no irrigation
The Anspach Effort, Inc.
12.4cm Heavy Duty Long Heavy Short Attachment Product Usage: Pneumatic system
The Anspach Effort, Inc.
RENOVATION, RADIAL OSTEOTOME BLADE, SIZE 16, REF 71369316, STERILE R, QTY: (1)
Smith & Nephew, Inc.
45 degree Contra Angle Attachment Product Usage: Pneumatic system
The Anspach Effort, Inc.
90 DEG RIGHT ANGLE ATTACH, BLACK MAX
The Anspach Effort, Inc.
Bearing Sleeve, 15CM Curved Product Usage: Pneumatic system
The Anspach Effort, Inc.
The JETSTREAM is a rotational atherectomy catheter system designed for use in debulking and treating vascular disease in the peripheral vasculature. …
Boston Scientific Corporation
IMRI CRANI-A ATTACHMENT Product Usage: Pneumatic system
The Anspach Effort, Inc.
RENOVATION, RADIAL OSTEOTOME BLADE, SIZE 10, REF 71369310, STERILE R, QTY: (1)
Smith & Nephew, Inc.
eMax2 Motor Assembly Product Usage: Electric system
The Anspach Effort, Inc.
16CM MIN INVASIVE ATTACH, BLACK MAX
The Anspach Effort, Inc.
AL-III-DISS Adapter Product Usage: Pneumatic system
The Anspach Effort, Inc.
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
DOLPHIN INFLATION DEVICE CALIBER INFLATION DEVICE; Catalog Number: CL3030- 018SNA- 018SND 0185NA 0185ND; INTERNAL CODE NUMBER: 0185TR- 0185NA- 018SND…
PEROUSE MEDICAL
11CM ANGLE ATTACHMENT, BLACK MAX
The Anspach Effort, Inc.
Schiller AG ISA CO2 Sensor (AKA: PhaseIn Unit), Merge Part Number HW-HEMO-00001. The PhaseIn Unit is an optional accessory (sold separately) to the …
Merge Healthcare, Inc.
Dressing Rect L, P/N 02428 Product Usage: These products are sterile dressings used as an insulation barrier between the Polar Care cold therapy …
Breg Inc
eMax2 Hybrid Hand Control Product Usage: Electric system
The Anspach Effort, Inc.
Compact Speed Reducer, 60:1 Black Max
The Anspach Effort, Inc.
Electronic Foot Control with Direction Switch Product Usage: Electric system
The Anspach Effort, Inc.
10.5cm QD Angle Attachment Product Usage: Pneumatic system
The Anspach Effort, Inc.
IMRI MOTOR Product Usage: Pneumatic system
The Anspach Effort, Inc.
Foot Control, SC2100 Product Usage: Electric system
The Anspach Effort, Inc.
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 …
Roche Diabetes Care, Inc.
22CM MICRO REVISION ATTACH, BLACK MAX
The Anspach Effort, Inc.
Autolube-III with NK Product Usage: Pneumatic system
The Anspach Effort, Inc.
RENOVATION, THIN OSTEOTOME BLADE, 8 MM X 5 INCH, REF 71369408, STERILE R, QTY: (1)
Smith & Nephew, Inc.
Electronic Foot Control with Direction or Irrigation Switches Product Usage: Electric system
The Anspach Effort, Inc.
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…
Beckman Coulter Inc.
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…
Zimmer Trabecular Metal Technology, Inc.
AL-III W/ male disconnect and 30ft hose Product Usage: Pneumatic system
The Anspach Effort, Inc.
RENOVATION, THIN OSTEOTOME BLADE, 10 MM X 3 INCH, REF 71369210, STERILE R, QTY: (1)
Smith & Nephew, Inc.
RENOVATION, THIN OSTEOTOME BLADE, 10 MM X 3 INCH, REF 71369410, STERILE R, QTY: (1)
Smith & Nephew, Inc.
Adult Craniotome Product Usage: Pneumatic system
The Anspach Effort, Inc.
RENOVATION, THIN OSTEOTOME BLADE, 12 MM X 3 INCH, REF 71369212, STERILE R, QTY: (1)
Smith & Nephew, Inc.
RENOVATION, THIN OSTEOTOME BLADE, 20 MM X 3 INCH, REF 71369220, STERILE R, QTY: (1)
Smith & Nephew, Inc.
20.2cm Heavy Duty Long Heavy Short Attachment
The Anspach Effort, Inc.
5.0cm Heavy Duty Short Attachment
The Anspach Effort, Inc.
Sagittal MICRO-SAW
The Anspach Effort, Inc.
XMAX Motor (Pneumatic Drill System) Product Usage: Pneumatic system
The Anspach Effort, Inc.
Pediatric Craniotome
The Anspach Effort, Inc.
14cm QD Angle Attachment
The Anspach Effort, Inc.
If Hip, Sterile Polar Dressing P/N 10680 Product Usage: These products are sterile dressings used as an insulation barrier between the Polar Care…
Breg Inc
Dale Medical Stabilock Endotracheal Adhesive Base Product # 273 The Dale Stabilock Endotracheal Tube Bolder 270 is a 2 piece device consisting of …
Dale Medical Products, Inc.
Nearby Recall Years
Browse recalls from adjacent calendar years to see how federal enforcement volume has shifted over time.
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
Read our methodology — how this data is sourced, computed, and verified.