PlainRecalls

2018 Recalls

7,795 recalls · Page 53 of 156

2018 Recall Year Insight

Federal agencies issued 7,795 product recalls indexed by PlainRecalls in calendar year 2018. That represents about 7.66% of the 101,704 total recalls we track from 1995 through the present, and averages roughly 21.4 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 156 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 2018.

On this page of 50 records, severity classification shows 4 critical, 45 moderate, and 1 lower-severity recalls. The page references 28 distinct recalling firms operating in 5 distinct product categories, with 34 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (42), CPSC (5), NHTSA (3), 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 2018 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 Aug 29, 2018

Pediatric Two-Lumen Central Venous Catheterization Kit with Blue FlexTip ARROWg+ard Blue Catheter, Cat. No. AK-22502 Product Usage: The multip…

Arrow International Inc

FDA Devices Moderate Aug 29, 2018

Vertebral Motion Analyzer (VMA), 2.3.239 - 2.3.254. Product Usage: VMA software is a quantitative imaging software application intended to be use…

Ortho Kinematics, Inc

FDA Devices Moderate Aug 29, 2018

Hitachi Scenaria CT system Product Usage: The SCENARIA CT system is indicated for head, whole body, cardiac and vascular X-ray Computed Tomograph…

Hitachi Medical Systems America Inc

FDA Devices Moderate Aug 29, 2018

DigitalDiagnost, Single-Detect (Stitching Patient Support) 712062

Philips Medical Systems Gmbh, DMC

FDA Devices Moderate Aug 29, 2018

DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712082

Philips Medical Systems Gmbh, DMC

FDA Devices Moderate Aug 29, 2018

BD BBL GC-Lect Agar; Cat. No. 297715 The device is a selective medium providing enhanced growth and recovery of Neisseria gonorrhoeae and better …

Becton Dickinson & Co.

FDA Devices Moderate Aug 29, 2018

Vertebral Motion Analyzer (VMA), 2.3.250. Product System, image processing, radiological

Ortho Kinematics, Inc

FDA Devices Moderate Aug 29, 2018

DigitalDiagnost Release 3.1 (Stitching Patient Support) 712026

Philips Medical Systems Gmbh, DMC

FDA Devices Moderate Aug 29, 2018

3D TOP Ceiling Stand, model no. 3070039 3074486 3070013 3070021 Product Usage: The ceiling stand is used to hold the X-ray tube and / or the d…

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Aug 29, 2018

GE Healthcare Optima CT660. Sold under the following product names: BEIJING OPTIMA CT660 PRO GT170, BEIJING OPTIMA CT660 PRO GT200, BEIJING O…

GE Healthcare Japan Corporation

FDA Devices Moderate Aug 29, 2018

Handicare C Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.

Handicare Usa Inc

FDA Devices Moderate Aug 29, 2018

DigitalDiagnost 4 Chest / Emergency (Stitching Patient Support) 712029

Philips Medical Systems Gmbh, DMC

FDA Devices Moderate Aug 29, 2018

O-Two Equinox¿ Relieve N2O/O2 Analgesic Gas Mixing and Delivery System Model#: 01EQ1000

O-Two Medical Technologies, Inc.

FDA Devices Moderate Aug 29, 2018

Philips SureSigns VS2 monitor, 863079 863080 863081 863082 863283 863286 The Sure Signs VS2 vital signs monitor is for use by healthcare pro…

Philips Electronics North America Corporation

FDA Devices Moderate Aug 29, 2018

EasyDiagnost Eleva DRF, Release 5 (Stitching Patient Support) 706050

Philips Medical Systems Gmbh, DMC

FDA Devices Moderate Aug 29, 2018

Vertebral Motion Analyzer (VMA), VMA DataLink Software.2.3.231, 2.3.232. Product Usage: VMA software is a quantitative imaging software applicat…

Ortho Kinematics, Inc

FDA Devices Moderate Aug 29, 2018

Liebel-Flarsheim Direct Digital Imaging System (DDIS) Liebel-Flarsheim urology systems facilitate radiologic and/or fluoroscopic procedures requi…

LIEBEL-FLARSHEIM COMPANY LLC

FDA Devices Moderate Aug 29, 2018

DigitalDiagnost 4.1 (Stitching Patient Support) 712225

Philips Medical Systems Gmbh, DMC

FDA Devices Moderate Aug 29, 2018

DigitalDiagnost Classic 1.x Upgrades (Stitching Patient Support) 712081

Philips Medical Systems Gmbh, DMC

FDA Devices Moderate Aug 29, 2018

MOSAIQ Oncology Information System

Elekta, Inc.

FDA Devices Moderate Aug 29, 2018

CoLink(TM) Lapidus Plate XP, +2 mm, Right, REF P40 ST165, QTY 1, In2Bones Product Usage: The In2Bones USA LLC, CoLink¿ Plating System is indicat…

In2bones USA, LLC

FDA Devices Moderate Aug 29, 2018

CombiDiagnost R90 (Stitching Patient Support) 709030

Philips Medical Systems Gmbh, DMC

FDA Devices Moderate Aug 29, 2018

Handicare P600 Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.

Handicare Usa Inc

FDA Devices Moderate Aug 29, 2018

DigitalDiagnost Classic, Dual-Detector (Stitching Patient Support) 712052

Philips Medical Systems Gmbh, DMC

FDA Devices Moderate Aug 29, 2018

Philips SureSigns VS3 Vital Signs Monitor, 863069 863070 863071 863072 863073 863074 The SureSigns VS3 monitor is for monitoring, recording a…

Philips Electronics North America Corporation

FDA Devices Moderate Aug 29, 2018

Stryker T2 ANKLE ARTHRODESIS NAIL RIGHT 10MMX200MM Item Number: 1819-1020S T2 ANKLE ARTHRODESIS NAIL RIGHT 12MMX200MM 1819-1220S T2 LONG PROXIMAL H…

Stryker GmbH

FDA Devices Moderate Aug 29, 2018

DigitalDiagnost Dual Detector (Stitching Patient Support) 712022

Philips Medical Systems Gmbh, DMC

FDA Devices Moderate Aug 29, 2018

CoLink(TM) Lapidus Plate XP, +2 mm, Left, REF P40 ST265, QTY 1, In2Bones Product Usage: The In2Bones USA LLC, CoLink¿ Plating System is indicate…

In2bones USA, LLC

FDA Devices Moderate Aug 29, 2018

DigitalDiagnost 4 Flex / Value (Stitching Patient Support) 712028

Philips Medical Systems Gmbh, DMC

FDA Devices Moderate Aug 29, 2018

Artholine Punch B 4, 6MM H 1, 6MM, used for the removal of soft tissue, cartilage tissue or other non-osseous tissue via natural or surgically creat…

Richard Wolf GmbH

FDA Devices Moderate Aug 29, 2018

GE Healthcare Revolution EVO, Optima CT660, Optima CT670, Optima CT680. The systems are intended for head, whole body, cardiac and vascular X-ray Co…

GE Healthcare Japan Corporation

FDA Devices Moderate Aug 29, 2018

Vertebral Motion Analyzer (VMA) Version 2.3.252. VMA software is a quantitative imaging software application intended to be used to process digit…

Ortho Kinematics, Inc

FDA Devices Moderate Aug 29, 2018

DigitalDiagnost, Dual-Detector (Stitching Patient Support) 712052

Philips Medical Systems Gmbh, DMC

FDA Devices Low Aug 29, 2018

is a quantitative/qualitative enzyme-linked immunosorbent assay (ELISA) for the detection of IgG and IgM autoantibodies specific for the phospholipid…

Euro Diagnostica AB

FDA Devices Moderate Aug 29, 2018

Connecting Bolt, Model 14-442093

Zimmer Biomet, Inc.

FDA Devices Moderate Aug 29, 2018

bioM¿rieux VITEK 2 NH ID Test Kit Product Usage: Is an automated system consisting of instruments, software and reagent cards designed for the ID…

Biomerieux Inc

FDA Devices Moderate Aug 29, 2018

Liebel-Flarsheim Hydra Vision Urology X-Ray System (DR) Liebel-Flarsheim urology systems facilitate radiologic and/or fluoroscopic procedures re…

LIEBEL-FLARSHEIM COMPANY LLC

FDA Devices Critical Aug 29, 2018

The Tri-Flo Subglottic Suction System

Vyaire Medical

FDA Devices Moderate Aug 29, 2018

DigitalDiagnost 4.1 High Performance (Stitching Patient Support) 712031

Philips Medical Systems Gmbh, DMC

FDA Devices Moderate Aug 29, 2018

GE Healthcare Optima CT540. The systems are intended for head, whole body, cardiac and vascular X-ray Computed Tomography applications.Sold under th…

GE Healthcare Japan Corporation

FDA Devices Moderate Aug 29, 2018

DigitalDiagnost Rel.4 Upgrades (Stitching Patient Support) 712084

Philips Medical Systems Gmbh, DMC

FDA Devices Moderate Aug 29, 2018

CAREstream ProNox Nitrous Oxide Delivery System labeled as the following: a. CMI-0100 PNX, Pro-Nox Mixer - Canadian; b. CMI-0100-PNX-HS, Pro…

CAREstream Medical LLC

CPSC Moderate Aug 29, 2018

BSN SPORTS Recalls Rubber Critter Toys Due to Violation of Federal Lead Paint Ban (Recall Alert)

BSN SPORTS LLC, of Farmers Branch, Texas

CPSC Moderate Aug 29, 2018

Cybex Recalls Weight-Lifting Equipment Due to Serious Injury Hazards

Cybex International Inc., of Owatonna, Minn.

NHTSA Critical Aug 29, 2018

TOYOTA 2012: AIR BAGS

TOYOTA

CPSC Moderate Aug 27, 2018

Polaris Recalls RZR XP Turbo S Recreational Off-Highway Vehicles Due to Injury Hazard (Recall Alert)

Polaris Industries Inc., of Medina, Minn

CPSC Moderate Aug 23, 2018

American Landmaster Recalls Off-Road Utility Vehicles Due to Fire and Burn Hazards

ASW, LLC d/b/a American Landmaster, of Columbia City, Ind.

CPSC Moderate Aug 23, 2018

Manhattan Toy Recalls Toy Planes Due to Choking Hazard

The Manhattan Toy Company LLC, of Minneapolis, Minn.

NHTSA Critical Aug 23, 2018

MINI 2017-2019: FUEL SYSTEM, GASOLINE:DELIVERY:FUEL PUMP

MINI

NHTSA Critical Aug 23, 2018

RAM 2018-2019: POWER TRAIN:AXLE ASSEMBLY

RAM

Nearby Recall Years

Browse recalls from adjacent calendar years to see how federal enforcement volume has shifted over time.

Compare 2018 with 2017 →

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 2018

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Figures cover calendar year 2018 across the FDA, CPSC 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 July 2026.