PlainRecalls

2017 Recalls

7,480 recalls · Page 122 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, 50 moderate, and 0 lower-severity recalls. The page references 6 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, 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

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 batter…

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 int…

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 …

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 …

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 PS…

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 …

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 …

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.

FDA Devices Moderate Mar 8, 2017

Facial Pack , part number AMS6501

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

BD AffirM VPIII Microbial Identification Test

Becton Dickinson & Co.

FDA Devices Moderate Mar 8, 2017

Plastic General Pack, part number AMS4215

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Extremity Pack-N Brunswick, part number PSS1866(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Brow Pack, part number PSS1785(C

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Angio Pack, part number AMS6711

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Morris Lap Pack, part number PSS3199(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Universal Pack, part number AMS2036

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Facial Plastic Pack, part number AMS3327(C

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Lap Gallbladder Pack, part number AMS3707

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Lower Extremity Pack, part number AMS4669

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: CPSC + NHTSA — consumer product and vehicle recall feeds for 2017