PlainRecalls

2018 Recalls

6,355 recalls · Page 69 of 128

2018 Recall Year Insight

Federal agencies issued 6,355 product recalls indexed by PlainRecalls in calendar year 2018. That represents about 7.57% of the 83,949 total recalls we track from 1995 through the present, and averages roughly 17.4 recalls per day across the FDA, CPSC, NHTSA, and USDA FSIS 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 128 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, 46 moderate, and 0 lower-severity recalls. The page references 18 distinct recalling firms operating in 3 distinct product categories, with 47 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (44), CPSC (3), 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, NHTSA, or USDA FSIS for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Devices Moderate Jun 6, 2018

MEDLINE O.R. Necessities(TM) Sterile* Needle Counter, 100 Ct. Double Magnet / Foam Block with Blade Remover, reorder: NC100FBR Product Usage: A n…

Medline Industries Inc

FDA Devices Moderate Jun 6, 2018

TheraCath(R) Epidural Catheter; Product Code: EC-05000

Arrow International Inc

FDA Devices Moderate Jun 6, 2018

7Fr. Catheter Clamp with Fastener; Product Code: CC-00007

Arrow International Inc

FDA Devices Moderate Jun 6, 2018

MagNA Pure 24 System, GMMI: 07290519001 Product Usage: The MagNA Pure 24 System is a fully automated clinical sample extractor. It extracts nucl…

Roche Molecular Systems, Inc.

FDA Devices Moderate Jun 6, 2018

Maximal Barrier Drape; Product Codes: ASK-00002-1A

Arrow International Inc

FDA Devices Moderate Jun 6, 2018

Medical Action Industries Inc. Blue OR Towel Non X-Ray Detectable (6 Towels per Pack) / product # AVID266 Sterile This OR towel product is intende…

Medical Action Industries Inc

FDA Devices Moderate Jun 6, 2018

Single-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Catheter and Sharps Safety Features; Product Codes: ASK-04301-TJ

Arrow International Inc

FDA Devices Moderate Jun 6, 2018

Respire Pink H/S Oral Sleep Apnea Device

Respire Medical

FDA Devices Moderate Jun 6, 2018

5Fr. Catheter Clamp with Fastener; Product Code: CC-00005

Arrow International Inc

FDA Devices Moderate Jun 6, 2018

ARROW JACC with Chlorag+ard Technology; Product Code: JR-42063-HPHNM and JR-42563-HPHNM

Arrow International Inc

FDA Devices Moderate Jun 6, 2018

ARROWg+ard Blue(R) MAC(TM) Two-Lumen Central Venous Access Kit for use with 7-7.5 Fr. Catheters; Product Code: ASK-21142-WHC2

Arrow International Inc

FDA Devices Moderate Jun 6, 2018

SOMATOM go.Now, Material Number 11061618 There is a potential for a software issue that may cause the need for necessary patient rescans.

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jun 6, 2018

LINX Reflux Management System, Implant Clasp, 12-17 Bead, 0.7T, Product Code LXC-xx, sterile, Rx only. Labeled as: a. Product Code LXC-12; b. …

Torax Medical, Inc.

FDA Devices Moderate Jun 6, 2018

Percutaneous Sheath Introducer Kit with ARROWgard Blue¿ Sheath and Integral Hemostasis Valve/Side Port for use with 7 - 7.5 Fr. Catheters; Product C…

Arrow International Inc

FDA Devices Moderate Jun 6, 2018

MEDLINE O.R. Necessities(TM) Sterile* Needle Counter, 40 Ct. Double Magnet / Foam Block with Blade Remover, reorder: NC100FBR Product Usage: A ne…

Medline Industries Inc

FDA Devices Moderate Jun 6, 2018

LINX Reflux Management System, Implant Suture, 12-17 Bead, 0.7T, Product Code LS-xx, sterile, Rx only. Labeled as: a. Product Code LS-12; b. P…

Torax Medical, Inc.

FDA Devices Moderate Jun 6, 2018

nordicTumorEx 1.0 nordicTumorEx is an image processing software package to be used by trained professionals including but not limited to physici…

NordicNeuroLab AS

FDA Devices Moderate Jun 6, 2018

MAC(TM) Two-Lumen Central Venous Access Kit with ARROWg+ard Blue(R) Access Device, Integral Hemostasis Valve and Sharps Safety Features for use with …

Arrow International Inc

FDA Devices Moderate Jun 6, 2018

Percutaneous Sheath Introducer Kit with ARROWg+ard Blue(R) Sheath, Integral Hemostasis Valve/Side Port, Sharps Safety Features, and Maximal Barrier P…

Arrow International Inc

FDA Devices Moderate Jun 6, 2018

Syva¿ EMIT¿ 2000 Theophylline Product Usage: The Syva¿ Emit¿ 2000 Theophylline Assay is a homogeneous enzyme immunoassay intended for use in the …

Siemens Healthcare Diagnostics, Inc.

FDA Devices Critical Jun 6, 2018

Heartware Medtronic HVAD System for cardiac use. Including the following parts: (a) Controller / Controller Kits, Product numbers: 1400, 1401, 140…

Heartware

FDA Devices Moderate Jun 6, 2018

Sheath Adapter with Cath-Gard¿ Catheter Contamination Shield for use with 4 - 7 Fr. Catheters; Product codes: SA-09847

Arrow International Inc

FDA Devices Moderate Jun 6, 2018

Arterial Catheterization Kit; Product Codes: ASK-04020-DH

Arrow International Inc

FDA Devices Moderate Jun 6, 2018

Gyrus ACMI Reusable Active Cord for Bovie/ValleyLab Generators, Catalog No C650-129A (00821925008700) The cord consists of a single conductor stra…

Gyrus Acmi, Incorporated

FDA Devices Moderate Jun 6, 2018

ARROWg+ard Blue PLUS¿ Pressure Injectable Two-Lumen CVC Kit; Product Code: CDC-42802-P1A

Arrow International Inc

FDA Devices Moderate Jun 6, 2018

Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter, Sharps Safety Features, and Maximal Barrier Pr…

Arrow International Inc

FDA Devices Moderate Jun 6, 2018

Two-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Catheter and Sharps Safety Features; Product Code: ASK-15402-HOP

Arrow International Inc

FDA Devices Moderate Jun 6, 2018

Echogenic Introducer Needle; Product Code: AN-04318

Arrow International Inc

FDA Devices Moderate Jun 6, 2018

ARROWg+ard Blue¿ PSI Kit with Integral Hemostasis Valve/ Side Port for use with 7 - 7.5 Fr. Catheters; Product codes: SF-29803-1

Arrow International Inc

FDA Devices Moderate Jun 6, 2018

Clear Fenestrated Drape with Adhesive; Product Code: CD-00001

Arrow International Inc

FDA Devices Moderate Jun 6, 2018

Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter and Sharps Safety Features; Product Codes: ASK-…

Arrow International Inc

FDA Devices Moderate Jun 6, 2018

ARROW PICC Set; Product codes: PR-35563-HPHNL and PR-35563-HPHNM

Arrow International Inc

FDA Devices Moderate Jun 6, 2018

Arrow PICC with Chlorag+ard Technology; Product codes: PR-44041-BAS, PR-44052-BAS, PR-44063-BAS, PR-45041-BAS, PR-45052-BAS, PR-45063-BAS, PR-45541-…

Arrow International Inc

FDA Devices Moderate Jun 6, 2018

Catheter Hemostasis Valve For use with .038" (.096 cm) dia. and smaller guide wires; Product Code: AI-07000

Arrow International Inc

FDA Devices Moderate Jun 6, 2018

Respire Pink+ Hard/Soft Oral Sleep Apnea Device

Respire Medical

FDA Devices Moderate Jun 6, 2018

ARROWgard Blue PLUS¿ Multi-Lumen CVC Kit with Blue FlexTip¿ Catheter; Product Code: MSO-45703-AHS

Arrow International Inc

FDA Devices Moderate Jun 6, 2018

9 Fr. Radiopaque Polyurethane Sheath/Dilator with Integral Hemostasis Valve/Side Port for use with 7 - 8 Fr. Catheters and Arrow Percutaneous Int…

Arrow International Inc

FDA Devices Moderate Jun 6, 2018

0.2 Micron Flat Epidural Filter; Product Code: EF-05500

Arrow International Inc

FDA Devices Moderate Jun 6, 2018

VOLISTA StandOP (model 600) surgical lights shipped from October 2012 until June 2017 equipped with keypads with Ref. ARD568801560; Part numbers: 568…

Maquet SAS

FDA Devices Moderate Jun 6, 2018

HeartStart MRx Monitor/Defibrillator, Model No. M3535A (861288), M3536A (861289) Product Automated external defibrillators (non-wearable) Produ…

Philips Electronics North America Corporation

FDA Devices Moderate Jun 6, 2018

Symmetry Olsen monopolar forceps: (a) Insulated Potts-Smith Forceps 8" (20.3cm) Serrated Tips, REF 20-2650K, QTY 10 (b) Insulated Bayonet Forceps …

Olsen Medical

FDA Devices Moderate Jun 6, 2018

nordicICE 2.3.14 Image processing software package used by trained professionals, including physicians and medical technicians.

NordicNeuroLab AS

FDA Devices Moderate Jun 6, 2018

Arrow-Johans" ECG Adapter for Right Atrial Electrocadiography (RAECG); Product Code: EG-04900

Arrow International Inc

FDA Devices Moderate Jun 6, 2018

Pressure Injectable Multi-Lumen Central Venous Catheterization Kit; Product Code: ASK-15703-PHMC

Arrow International Inc

CPSC Moderate Jun 6, 2018

GE Lighting Recalls LED Tube Lamps Due to Shock and Electrocution Hazards; Sold Exclusively at Lowe's Stores

CPSC Moderate Jun 6, 2018

Vernier Software & Technology Recalls Circuit Boards Due to Burn Hazard (Recall Alert)

Charles Assembly, of Aloha, Ore.

NHTSA Critical Jun 6, 2018

BMW 2018-2019: LANE DEPARTURE: LANE KEEP: STEERING ASSIST

BMW

CPSC Moderate Jun 5, 2018

Keyera Energy Recalls to Inspect Propane Gas Due to Fire and Explosion Hazards

Keyera Energy Inc., of Houston, Texas

NHTSA Critical Jun 4, 2018

AUDI 2012-2018: AIR BAGS:SENSOR:OCCUPANT CLASSIFICATION

AUDI

NHTSA Critical Jun 1, 2018

AUDI 2018: SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:DISC:CALIPER

AUDI

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 + USDA FSIS — consumer product, vehicle, and meat/poultry recall feeds for 2018