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 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, 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

Hysteroscopy Pack, part number AMS4797 Hysteroscopy Pack, part number AMS4797(A Hysteroscopy Pack, part number AMS4797(B

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Extremity Pack (1344), part number AMS6561

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Check-Flo Performer Introducer Set, 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

Chest Breast Drape, part number AMS5853

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Uretero-reno videoscope URF-V2 and URF-V2R endoscope and accessories The URF-V2/V2R endoscopes are intended for use in endoscopic diagnosis and treatment within the ureter and kidney.

Olympus Corporation of the Americas

FDA Devices Moderate Mar 8, 2017

Spine Pack , part number AMS3753(A Spine Pack, part number AMS3783(A Spine Pack, part number AMS3783(B Spine Pack, part number AMS6472

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

URF-P6 Uretero-reno fiberscope and URF-P6R Uretero-reno fiberscope

Olympus Corporation of the Americas

FDA Devices Moderate Mar 8, 2017

Shoulder Arthroscopy Pack, part number AMS2496(A Shoulder Arthroscopy Pack, part number AMS2496(B Shoulder Arthroscopy Pack, part number AMS2496(C Shoulder Arthroscopy Pack, part number AMS2609 Shoulder Arthroscopy Pack, part number AMS3857 Shoulder Arthroscopy Pack, part numbr AMS4766 Shoulder Arthroscopy Pack, part number AMS4766(A Shoulder Arthroscopy Pack, part number AMS4766(B

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

EliA Sample Diluent, Article number, 83-1023-01

Phadia US Inc

FDA Devices Moderate Mar 8, 2017

Basic Setup Pack, part number AMS1787(A Basic Setup Pack, part number AMS6519

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Basin Pack, part number AMS2497

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Upper Extremity Pack, part number AMS4670 Upper Extremity Pack, part number AMS4670(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Hystero Pack, part number PSS3535(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Pacemaker Kit, part number AMS4281 Pacemaker Kit, part number AMS4281(A Pacemaker Kit, part number AMS4281(C Pacemaker Kit, part number AMS4281(D

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Eye Tray, part number PSS1834 Eye Tray, part number PSS1834(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Catheter Pack, part number AMS4399(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

SONNET Mini Battery Pack CableProduct Usage: The SONNET Mini Battery Pack Cable is part of the SONNET Mini Battery Pack, which is an external battery pack used to power one MED-EL SONNET control unit. It can be worn on the upper body or the hip using different SONNET Mini Battery Pack Cable lengths to connect the SONNET Mini Battery Pack to one processor unit.

MED-EL Elektromedizinische Gereate, Gmbh

FDA Devices Moderate Mar 8, 2017

Check-Flo Introducer Hausdorf-Lock Atrial, 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

Lipo Pack, part AMS4420(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Ortho Minor Pack, part number AMS3710(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Lap/Pelviscopy Pack, part number PSS3256(B

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

General Laparoscopy Pack, part number AMS4798 General Laparoscopy Pack, part number AMS4798(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

D & C Pack, part number AMS4796(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Flexor Radial Access Set, Individual product is packaged in a Tyvek-film sterilizable outer pouch. The Flexor¿ Radial Hydrophilic Introducer Access Set is intended to introduce diagnostic and interventional devices In radial artery access procedures

Cook Inc.

FDA Devices Moderate Mar 8, 2017

CARDIOSAVE Hybrid IABP and CARDIOSAVE Rescue IABP affected part number is 0998-:XX-0800-XX Li-Ion Battery affected part number is 0146-00-0097 Product Usage: The CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP) is an electromechanical system used to inflate and deflate intra-aortic balloons

Maquet Datascope Corp - Cardiac Assist Division

FDA Devices Moderate Mar 8, 2017

General Plastic Pack, part number PSS2432(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Bleph Pack, part number AMS3325(B

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Basic Extended Pack, part number AMS4421(A Basic Extended Pack, part number AMS4421(B

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Vein Tray, part number AMS6312

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Custom Pack - with Introducer Kit, part number TVS4011NI(L

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

ENT Pack, part number AMS3237(A ENT Pack, part number AMS4214

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Plastic Surgery Pack, part number AMS5685

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Head Pack, part number PSS1934(B

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Arthroscopy Pack, part number AMS2938 Arthroscopy Pack, part number AMS3639 Arthroscopy Pack, part number AMS4765 Arthroscopy Pack, part number PSS1799 Arthroscopy Pack, part number PSS1845(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Podiatry Pack, part number AMS2778 Podiatry Pack, part number AMS2778(A Podiatry Pack, part number AMS3785(B Podiatry Pack, part number AMS3785(C Podiatry Pack, part number AMS4011(A Podiatry Pack, part number PSS3422(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Total Joint Pack, part number 006358-6

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Custom Breast Augmentation Pack, part number PSS2455(D

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

McKesson Radiology 12.2 - Picture Archive Communication System (PACS)

Mckesson Medical Imaging

FDA Devices Moderate Mar 8, 2017

GYN Lap Pack, part number PSS2194(B

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Hand Pack, part number AMS3640 Hand Pack, part number AMS4213(A Hand Pack, part number AMS4311(A Hand Pack, part number AMS5343 Hand Pack., part number PSS1843(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Peri GYN, part number PSS2193(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Set Up Pack, part number PSS3574(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Lumbar Laminectomy Pack, part number AMS2501 Lumbar Laminectomy Pack, part number AMS2501(A Lumbar Laminectomy Pack, part number AMS2501(B

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Basic Pack (1185), part number AMS6560

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Abdominoplasty Pack, Part numbers AMS3326(B, AMS4381, and AMS4381(B.

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Percutaneous Entry Kit, part number TVS4022(D Percutaneous Entry Kit , part number TVS4022(E Percutaneous Entry Kit, part number TVS4022(F

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Open Procedure Pack, part number AMS4596 Open Procedure Pack, part number AMS4596(A Open Procedure Pack, part number AMS4596(B

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Plastic Kit, part number CMP1084(C

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Dr Bragg Vein Tray - RX, part number 007912-8

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Dr. Landi EVLT Pack, part number AMS1483(E Dr. Landi EVLT Pack, part number AMS1483(E

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.