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, 49 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, 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 Mar 8, 2017

Eye Plastic Tray, part number PSS1931(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Robotic Pack, part number AMS4389

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Lap Band Pack, part number AMS1785(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Siemens ADVIA Centaur Systems Calibrator A Kits, Cat No. 04800646, SMN 10285903 (2 pack)Cat No. 04800735, SMN 10285904 (6 pack) Cat No. 04800840, SMN 10285905 (6 pack - REF)

Siemens Healthcare Diagnostics, Inc

FDA Devices Moderate Mar 8, 2017

Custom Pack, part number AMS4776 Custom Pack, part number AMS4776(A Custom Pack, part number AMS5643 Custom Pack, part number AMS5643(A Custom Pack, part number AMS6012 Custom Pack, part number AMS6383 Custom Pack, part number PSS2135(B Custom Pack, part number PSS2798(B Custom Pack, part number PSS2798(C Custom Pack, part number PSS3463

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Bayview Breast Pack, part number 009080-2

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Minor Pack, part number AMS3782(B Minor Pack, part number AMS3782(C Minor Pack, part number CMP1560 Minor Pack, part number PSS3518(B Minor Pack, part number PSS3541(A

Windstone Medical Packaging, Inc.

FDA Devices Critical Mar 8, 2017

Medtronic SynchroMed II Implantable Drug Infusion System. This system includes: Model 8870 Software Application Card, Model 8840 N'Vision Clinician Programmer, and Model 8637 SynchroMed II Implantable Drug Infusion Pump (supplied in 20 ml or 40 ml reservoir size.) Product Usage: The SynchroMed II Programmable Pump is indicated when patient therapy requires the chronic infusion of the following drugs or fluids: Chronic intraspinal (epidural and intrathecal) infusion of preservative-free

Medtronic Neuromodulation

FDA Devices Moderate Mar 8, 2017

Major Breast Pack, part number AMS3409(B

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Lap Chole Pack (6037) , part number AMS6567

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

D&C/Cysto Pack, part number PSS3257(D

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Hand Tray, part number PSS2365(F Hand Tray, part number PSS2365(G

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Facial Tray, part number PSS1558(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Knee Arthroscopy Pack , part number AMS2610(A Knee Arthroscopy Pack, part number AMS3236(A Knee Arthroscopy Pack, part numbre AMS3860

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Foot Pack, part number AMS3637

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Hip Pack (1347), part number AMS6564

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Minor Procedure Pack, part number AMS4799

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Breast Pack, part number AMS3238(A Breast Pack, part number AMS4419(A Breast Pack, part number AMS4419(B Breast Pack, part number AMS5750 Breast Pack, part number AMS5750(A Breast Pack, part number AMS6120 Breast Pack, part number PSS1784(B Breast Pack, part number PSS2272(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Check-Flo Hemostasis Assembly, Individual product is packaged in a Tyvek-film sterilizable outer pouch.

Cook Inc.

FDA Devices Moderate Mar 8, 2017

Laminectomy Pack, part number PSS1844(B

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Morris Hysto Pack, part number PSS3198(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Basic Face Kit, part number PS517A(D

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Dr. Newman Surgical Procedure Pack, part number PSS1689(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Check-Flo Performer Introducer, Individual product is packaged in a Tyvek-film sterilizable outer pouch. Introducers are intended for introduction of balloons, closed and non-tapered end catheters or other diagnostic and interventional devices.

Cook Inc.

FDA Devices Moderate Mar 8, 2017

Anterior Cervical Fusion Pack, part number AMS2502(A Anterior Cervical Fusion Pack, part number AMS2502(C

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Basic Kit, part number CMP1109(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Minor Tray, part number AMS2685

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Dr. Casey Pack, part number AMS4313(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Lap Minor Pack (1346), part number AMS6566

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Set-Up Pack, part number PSS1305(C

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Laparoscopic Pack, part number AMS2499 Laparoscopic Pack, part number AMS2499(A Laparoscopic Pack, part number AMS2499(B

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Open Procedure Pack II, part number RMS1740(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Basic Tray, part number PSS1559(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Head/Neck Pack, part number AMS6121

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Shoulder Pack, part number AMS2936 Shoulder Pack, part number AMS3638 Shoulder Pack, part number AMS3711(B Shoulder Pack, part numbere AMS4212 Shoulder Pack, part number AMS6460 Shoulder Pack, part numberPSS1852(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Siemens ADVIA Centaur Systems Calibrator A Kits, Cat No. 04800646, SMN 10285903 (2 pack)Cat No. 04800735, SMN 10285904 (6 pack) Cat No. 04800840, SMN 10285905 (6 pack - REF)

Siemens Healthcare Diagnostics, Inc

FDA Devices Moderate Mar 8, 2017

Knee Scope Pack, part number AMS2498(A Knee Scope Pack, part number AMS2498(B Knee Scope Pack, part number AMS2498(C

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

OP7543 Design Y Mandible Onlay - Medium - Left and OP7544 Design Y Mandible Onlay - Medium - Right

Matrix Surgical Holdings, LLC

FDA Devices Moderate Mar 8, 2017

Extremity Pack, part number AMS3240 Extremity Pack, part number AMS4764 Extremity Pack, part number AMS4788(A Extremity Pack, part number PSS1798(A Extremity Pack, part number PSS1798(A Extremity Pack, part number PSS1798(A Extremity Pack, part number PSS1842(A Extremity Pack, part number PSS1842(A Extremity Pack, part number PSS1842(A Extremity Pack, part number PSS1842(A Extremity Pack, part number PSS2706 Extremity Pack, part number PSS2706 Extremity Pack, part number PSS2706 Ext

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Reduction Mammoplasty Pack, part number AMS4380 Reduction Mammoplasty Pack, part number AMS4380(B

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Augmentation Pack, part number AMS6370

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

PRODISC Orthopedic Manual Surgical Instrument, strut used in spinal surgery. Part numbers 03.820.350 and 03.820.352. Used to hold the disc segment open and facilitate discectomy

Synthes (USA) Products LLC

FDA Devices Moderate Mar 8, 2017

General Plastics Pack, part number 008617-1

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Liposuction Pack, part number AMS3323(B Liposuction Pack, part number AMS5684 Liposuction Pack, part number AMS5699

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Total Knee Pack (15710), part number AMS6563

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

GYN Pack, part number AMS4013(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

iChemVELOCITY Urine Chemistry System, Catalog No. 800-3530, 800-7167, 800-7719, 800-7720, 800-3564, 800-7100, 800-7103, 800-7106, 800-7162, 800-7163, 800-7166, 800-3061. The iChem Velocity automated urine chemistry system is used to test for the following analytes in urine: ketones, blood, protein, glucose, bilirubin, urobilinogen, nitrite, leukocyte esterase, specific gravity, pH, ascorbic acid, color, and clarity. The iChem Velocity automated urine chemistry analyzer is intended to be used fo

Beckman Coulter Inc.

FDA Devices Moderate Mar 8, 2017

Lap Pack, part number AMS4801

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Ocular Plastic Pack, part number AMS3868(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Opgrande Hand Pack, part number AMS4767

Windstone Medical Packaging, 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.