PlainRecalls

2018 Recalls

Compiled from official public sources by the editorial team.

7,717 recalls · Page 130 of 155

2018 Recall Year Insight

Federal agencies issued 7,717 product recalls indexed by PlainRecalls in calendar year 2018. That represents about 7.70% of the 100,165 total recalls we track from 1995 through the present, and averages roughly 21.1 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 155 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 11 critical, 38 moderate, and 1 lower-severity recalls. The page references 34 distinct recalling firms operating in 6 distinct product categories, with 40 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (30), NHTSA (10), CPSC (9), 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 Mar 7, 2018

Axiom Artis model Interventional fluoroscopic x-ray foot switch accessory; Model Numbers: 4787797, 4787805, and 4787813.

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Mar 7, 2018

NxStage Dialysate Sack: 1) REF SAK-301 UDI-M535SAK3010, 2) REF SAK-302 UDI-M535SAK3020, 3) REF SAK-303 UDI-M535SAK3030, 4) REF SAK-304 UDI-M535SAK304…

NxStage Medical, Inc.

FDA Devices Moderate Mar 7, 2018

MOOG Curlin Infusion Administration Set, Ref 340-4168, Non-DEHP Microbore Tubing with Non-Vented Bag Spike and distal Female Luer Y-Site with Check V…

Zevex Incorporated (dba Moog Medical Medical Devices Group)

FDA Devices Moderate Mar 7, 2018

STAT 2¿ I.V. Gravity Flow Needle-Free Controller Primary Administration Sets and Extension Sets (Catalog Numbers: (1) S2-12 N, STAT 2¿ Extension Set …

ConMed Corporation

FDA Devices Low Mar 7, 2018

JANUS & JANUS G3 Automated Workstation is an automated programmable liquid handling instrument intended for use in clinical settings to facilitate t…

Perkinelmer Life Sciences, Inc.

FDA Devices Moderate Mar 7, 2018

The 2nd Assist Knee Positioner

Zimmer Biomet, Inc.

FDA Devices Moderate Mar 7, 2018

Truth Renew Plus

Accord Media, LLC

FDA Devices Moderate Mar 7, 2018

Versys 6 inch Beaded Full Coat Plus Hip Prosthesis. Labeled as follows: a. VERSYS 6 INCH BEADED FC 19X160MM STD BODY STD NECK (Item No. 008943019…

Zimmer Biomet, Inc.

FDA Devices Moderate Mar 7, 2018

Vis-U-All High Temperature Tubing 6"x100'. One roll per box; 10 boxes per case 10 rolls/cs Product Usage: The Vis-U-All High Temperature Sterilizat…

Steris Corporation

FDA Devices Critical Mar 7, 2018

ultraView SISH Detection Kit, Ventana Part Number 780-001, Roche GMMI 05271967001 in vitro diagnostic

Ventana Medical Systems Inc

FDA Devices Moderate Mar 7, 2018

Vis-U-All High Temp 10.5"x28" Self Seal Pouch 100 pouches per box; 4 boxes per case Product Usage: The Vis-U-All High Temperature Sterilization P…

Steris Corporation

FDA Devices Moderate Mar 7, 2018

Syngo.via systems with SW VB20A

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Mar 7, 2018

ProLite Mesh - mesh, surgical, polymeric ProLite Mesh is intended for use in soft tissue deficiencies including hernia repair, traumatic or surgic…

Atrium Medical Corporation

FDA Devices Moderate Mar 7, 2018

Phoenix Antegrade Femoral Nail Trochanteric and Piriformis fossa, Model#14-442093 Antegrade Femoral Connecting Bolt. orthopedic instrument

Zimmer Biomet, Inc.

FDA Devices Moderate Mar 7, 2018

AVID TruCustom LAMINECTOMY PACK convenience kits, Item Code: MADN013-02

Avid Medical, Inc.

FDA Devices Moderate Mar 7, 2018

Better-Bladder cardiopulmonary bypass blood reservoir; Models: BB14 (individual, sterile, pouched) and BB14NS (sold bulk to kit manufacturers)

Circulatory Technology Inc

FDA Devices Moderate Mar 7, 2018

Vis-U-All High Temp 8"x16" Self Seal Pouch 200 pouches per box; 4 boxes per case Product Usage: The Vis-U-All High Temperature Sterilization Pouc…

Steris Corporation

FDA Devices Moderate Mar 7, 2018

Vis-U-All High Temperature Tubing 4"x100'. One roll per box; 10 boxes per case 10 rolls/cs Product Usage: The Vis-U-All High Temperature Steriliz…

Steris Corporation

FDA Devices Moderate Mar 7, 2018

MOOG Curlin Infusion Administration Set, Ref 340-4114, Non-DEHP Microbore Tubing with Non-Vented Bag Spike, packaged 20/box, for use with the MOOG Cu…

Zevex Incorporated (dba Moog Medical Medical Devices Group)

FDA Devices Moderate Mar 7, 2018

Vis-U-All High Temp 5.5"x10" Self Seal Pouch 200 pouches per box; 4 boxes per case Product Usage: The Vis-U-All High Temperature Sterilization Po…

Steris Corporation

FDA Devices Moderate Mar 7, 2018

AVID TruCustom ELECTRO PHYSIOLOGY PK convenience kits, Item Code: LGHM033-04

Avid Medical, Inc.

FDA Devices Moderate Mar 7, 2018

ST AIA-PACK¿ PROG II, Progesterone II Assay, Part Number: 025239

Tosoh Bioscience Inc

FDA Devices Moderate Mar 7, 2018

Berchtold Chromophare Ceiling Mounted Surgical Light System, Catalog #CH13000000. Product Usage: Chromophare surgical lights are medical lights f…

Stryker Communications

FDA Devices Moderate Mar 7, 2018

Ultra Renew

Accord Media, LLC

FDA Devices Moderate Mar 7, 2018

2008T, Hemodialysis Delivery System Product Indicated for acute and chronic dialysis therapy.

Fresenius Medical Care Renal Therapies Group, LLC

FDA Devices Moderate Mar 7, 2018

Stage-1¿ RDS Indexed Abutment for RDS Stage-1¿ Single Stage Implants Keystone s implants are intended for use in partially or fully edentulou…

Keystone Dental Inc

FDA Devices Moderate Mar 7, 2018

AVID TruCustom PACEMAKER TRAY convenience kits, Item Code: LAKC020-08 and LAKC020-09

Avid Medical, Inc.

FDA Devices Moderate Mar 7, 2018

AVID TruCustom PV MINOR PACK convenience kits, Item Code: MADN017-02 and MADN017-03

Avid Medical, Inc.

FDA Devices Moderate Mar 7, 2018

Artis Zee and Zeego, Model Numbers: 10094135, 10094137, 10094141, 10094142, 10094143, 10280959, 10848283 & 10848354

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Mar 7, 2018

Vis-U-All High Temperature Tubing 14"x100'. One roll per box; 10 boxes per case 6 rolls/cs Product Usage: The Vis-U-All High Temperature Steriliz…

Steris Corporation

CPSC Moderate Mar 7, 2018

First Aid Research Recalls Maximum Strength Bacitraycin Plus Ointment With Lidocaine Due to Failure to Meet Child Resistant Closure Requirement

First Aid Research Corp., of Jupiter, Fla.

CPSC Moderate Mar 7, 2018

Husqvarna Motorcycles Recalls Closed Course Competition Motorcycles Due to Crash Hazard (Recall Alert)

KTM AG, Austria

CPSC Moderate Mar 7, 2018

Topson Downs Recalls Cat & Jack Girls' Star Studded Jeans Due to Laceration Hazard; Sold Exclusively at Target

Topson Downs, of Culver City, Calif.

NHTSA Critical Mar 7, 2018

NISSAN 2011-2012: FUEL SYSTEM, GASOLINE

NISSAN

NHTSA Critical Mar 7, 2018

BMW 2018: STRUCTURE:BODY

BMW

CPSC Moderate Mar 6, 2018

InSinkErator® Recalls SinkTop™ Switch Accessory for Garbage Disposals Due to Fire Hazard

Tecmark of Mentor, Ohio

CPSC Moderate Mar 6, 2018

Woodstream Recalls Mosquito Magnet Traps Due to Injury Hazard

Woodstream Corporation, of Knoxville, Tenn.

NHTSA Critical Mar 6, 2018

NISSAN 2018: AIR BAGS:SIDE/WINDOW

NISSAN

NHTSA Critical Mar 6, 2018

MACK 2018: VISIBILITY:WINDSHIELD WIPER/WASHER

MACK

NHTSA Critical Mar 6, 2018

MERCEDES-BENZ 2017: EXTERIOR LIGHTING:HEADLIGHTS

MERCEDES-BENZ

NHTSA Critical Mar 6, 2018

MERCEDES-BENZ 2018: SEATS:FRONT ASSEMBLY:RECLINER

MERCEDES-BENZ

NHTSA Critical Mar 6, 2018

ALFA ROMEO 2018: VISIBILITY:WINDSHIELD WIPER/WASHER:MOTOR

ALFA ROMEO

CPSC Moderate Mar 5, 2018

Goodman Manufacturing Recalls Modular Blowers Due to Fire Hazard

Goodman Manufacturing Company, L.P., of Houston, Texas

CPSC Moderate Mar 1, 2018

Double Insight Recalls Multicookers Due to Fire Hazard; Sold Exclusively at Walmart

Foshan Linshine Technology Co., Guangdong, China

CPSC Moderate Mar 1, 2018

Goodman Company Recalls Packaged Terminal Air Conditioners and Heat Pumps Due to Burn and Fire Hazards

Goodman Company, L.P. of Houston, Texas

CPSC Moderate Mar 1, 2018

Graco Recalls Highchairs Due to Fall Hazard; Sold Exclusively at Walmart

Wonderland Nursery Goods Co., LTD, of Dongguan Guangdong, China

NHTSA Critical Mar 1, 2018

FORD 2017-2018: ELECTRICAL SYSTEM:IGNITION

FORD

NHTSA Critical Mar 1, 2018

JAGUAR 2018: SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:HOSES, LINES/PIPING, AND FITTINGS

JAGUAR

NHTSA Critical Mar 1, 2018

LAND ROVER 2018: VISIBILITY:DEFROSTER/DEFOGGER/HVAC SYSTEM

LAND ROVER

FDA Food Moderate Feb 28, 2018

Flexfrost Protein Ice Cream Mint Chip Flexfrost L.L.C. 622 RT 10 Whippany, NJ 07981

Flexfrost

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