PlainRecalls

2018 Recall Year Insight

Federal agencies issued 7,928 product recalls indexed by PlainRecalls in calendar year 2018. That represents about 7.59% of the 104,423 total recalls we track from 1995 through the present, and averages roughly 21.7 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 159 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 6 critical, 38 moderate, and 6 lower-severity recalls. The page references 24 distinct recalling firms operating in 4 distinct product categories, with 47 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (35), FDA Food (14), FDA Drug (1), 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, USDA FSIS, or NHTSA for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Food Critical Jul 4, 2018

Utz Organic Yellow Corn Tortillas, Net Wt 9 oz; UTZ Quality Foods, Inc., Hanover, PA 17331; UPC: 0-41780-01337-8; Exp date: MAY 26 18 to JUN 16 18;

Utz Quality Food Inc

FDA Food Low Jul 4, 2018

Belly Fat Reducer + Energy Booster and Stamina, Dietary Supplement

Nutreglo Products, LLC.

FDA Food Low Jul 4, 2018

Honey Oat Bran Muffin, 4-pack, packaged in a clear clamshell container, net wt. 13.6 oz., UPC 8 40600 10954 9

New Seasons Market LLC

FDA Food Moderate Jul 4, 2018

Blueberry Buckwheat Muffin, 4-pack, packaged in a clear clamshell container, net wt. 13.6 oz., UPC 8 40600 10952 5

New Seasons Market LLC

FDA Food Critical Jul 4, 2018

Weis Signature Collection No Salt Added White Corn Tortilla Chips; Net Wt 11 oz; Manufactured For Weis Markets, Sunbury, PA 17801; UPC: 0-41497-00427-0; Exp date: May 26 18 to JUN 16 18;

Utz Quality Food Inc

FDA Food Low Jul 4, 2018

Pacific Brand Charcoal Grilled Eel. Premium Quality Unagi Kabayaki UPC: 692156201099

Supreme Foods

FDA Food Critical Jul 4, 2018

Golden Flake TORTIYAHS! Superior Dipping Chips; Net Wt 12.5 oz Tortilla Chips; Golden Flake Snack Foods, Inc. Birmingham, AL 35201; UPC: 0-72080-41000-0; Exp date: JUN 2 18 to JUN 23 18;

Utz Quality Food Inc

FDA Food Moderate Jul 4, 2018

BLUEBERRY PRETZEL, NET WEIGHT : 4OZ (113g) ,USE BY DATE : 12/1/2018

Four Link Nutriworld

FDA Food Critical Jul 4, 2018

Utz Organic Blue Corn Tortillas; Net Wt 9 oz; UTZ Quality Foods, Inc., Hanover, PA 17331; UPC: 0-41780-01317-0; Exp date: JUN 16 18;

Utz Quality Food Inc

FDA Food Critical Jul 4, 2018

Mini Butter Croissants, 8-Pack, packaged in a clear plastic clam-shell container, net wt. 6 oz., UPC 8 40600 10904 4

New Seasons Market LLC

FDA Food Critical Jul 4, 2018

Good Health Organic Tortillas; Black Bean & Rice; Net Wt 5.5 oz; Distributed by Good Health Natural Products, Inc. Greensboro, NC; UPC: 274077-55355-04100-9; Exp date: DEC 29 18; Mexico only: Good Health Totopos Organicos; Frijol Negro y Arroz; Cont. Neto 538,6 g; Distribuido por Good Health Natural Products, Inc.; 900 High St, Hanover, PA 17331; Importado por: Importadora Primex, S.A. de C.V. Blvd. Magnocentro No. 4, San Fernando La Herradura Hulxqullucan, Estado de M¿xico, C.P. 52765; ITM

Utz Quality Food Inc

FDA Food Low Jul 4, 2018

Vegan Chocolate Almond Muffin, 4-pack, packaged in a clear clamshell container, net wt. 13.6 oz., UPC 8 40600 10955 6

New Seasons Market LLC

FDA Food Low Jul 4, 2018

Lyfetrition Live Life Nutritiously Vitamin B12 2 FL. OZ bottle Supplement Facts Serving Size:***Vitamin B-12 (as Methylcobalamyn) ABSONUTRIX 5500 Adams Farm Lane, Suite 206 Greensboro NC 27407 UPC 7 00443 88822 6

Absonutrix

FDA Food Low Jul 4, 2018

McEvoy Ranch 100% Certified Extra VirginOlive Oil; Made in California; 1 L, 33,8 FL OZ UPC 6 34832 00291

McEvoy of Marin, LLC.

FDA Drug Moderate Jul 4, 2018

fentanyl Citrate USP 5 mcg in 0.9% Sodium Chloride USP 0.5 mL, 10 mcg per mL prefilled syringe, Rx only, Advanced Pharma an FDA Regulated 503B Outsourcing Facility 9265 Kirby Dr., Houston, TX 77054, NDC 15082-210-72.

Advanced Pharma Inc.

FDA Devices Moderate Jul 4, 2018

Brilliance Big Bore Radiology 728244

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Jul 4, 2018

CS-7, Model No. A4C1

Konica Minolta Medical Imaging USA, Inc.

FDA Devices Moderate Jul 4, 2018

Merlin PCS programmer (Model # 3650), Software (Model # 3330)

St Jude Medical Inc.

FDA Devices Moderate Jul 4, 2018

ABX Pentra Micro ALBUMIN 2 CP, Serum/Plasma, REF 1300032563 The device is intended for use in conjunction with certain materials to measure a variety of analytes.

Horiba Instruments, Inc dba Horiba Medical

FDA Devices Moderate Jul 4, 2018

VIDAS FSH, Ref 30407-01, IVD, Rx. The firm name on the label is bioMerieux SA, France. For use on the instruments of the VIDAS family (VITEK ImmunoDiagnostic Assay System) as an automated quantitative enzyme-linked fluorescent immunoassay (ELFA) for the determination of human follicle stimulating hormone (FSH) concentration in human serum or plasma (heparin). It is intended for use as an aid in the diagnosis of pituitary gland and gonadal disorders.

BioMerieux SA

FDA Devices Moderate Jul 4, 2018

Unify, Sterile EO, Model #/ Part #: CD3231-40/100029240, 100030104, 100041904; CD3231-40Q/100029281, 100030124, 100041905; CD3235-40/100029256, 100029293, 100029307, 100031111, 100037047, 100048897, 100070009; CD3235-40Q/100029257, 100029294, 100029308, 100031059, 100037048, 100070010; CD3281-40Q/100056770; CD3297-40/100056933

St Jude Medical Inc.

FDA Devices Moderate Jul 4, 2018

Artis Q.zen floor, Material no. 10848353, for angiography and whole body radiographic/fluoroscopic procedures.

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 4, 2018

Artis Q.zeego, Material no. 10848283, for angiography and whole body radiographic/fluoroscopic procedures.

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 4, 2018

Philips Ingenuity Core 728321

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Jul 4, 2018

Randox Liquid Assayed Specific Protein Control - Level 2 (SP Control 2), Cat. no. PS2683

Randox Laboratories Ltd.

FDA Devices Moderate Jul 4, 2018

Ingenuity Core128 728323

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Jul 4, 2018

Artis Q biplane, Material no. 10848282, for angiography and whole body radiographic/fluoroscopic procedures.

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 4, 2018

Fortify, Sterile EO, Model #/ Part #: CD1231-40/100029238,100030095, 100041981; CD1231-40Q/100029229, 100030087, 100041982; CD1233-40/100029230, 100029250, 100029259,100031058, 100059778, 100070017; CD1233-40Q/100029260, 100029271, 100029277, 100031104, 100070089; CD1235-40/100029272, 100029282, 100029311, 100031039, 100059779; CD1235-40Q/100029273, 100029295, 100029312, 100030840; CD1241-40/100046351; CD1241-40Q/100046167; CD2231-40/100029274, 100030110, 100041922; CD2231-40

St Jude Medical Inc.

FDA Devices Moderate Jul 4, 2018

Space Pump IV Set, 2 Caresites, ASV, 0.2 Micron Air Eliminating Filter, Product Code 363420 The Infusomat Space Pump IV Set, 2 Caresites, ASV with 0.2 Micron Air Eliminating Filter and Anti-Syphon Valve (ASV) is a latex-free product intended to be used with the Infusomat Space Pump, to deliver intravenous solutions. The 0.2 Micron filter is a clear acrylic in-line filter designed to eliminate air within the IV infusion set. While it is not listed in the labeling, it is known that the filter i

B. Braun Medical, Inc.

FDA Devices Moderate Jul 4, 2018

Artis Q ceiling, Material no. 10848281, for angiography and whole body radiographic/fluoroscopic procedures.

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 4, 2018

Fortify Assura, Sterile EO, Model #/ Part #: CD1257-40/100042322, 100059623; CD1257-40Q/100042341, 100059535; CD1259-40/100041914, 100042338, 100059536, 100059646, 100081567; CD1259-40Q/100041931, 100042339, 100059537, 100059620, 100059626, 100078685; CD1263-40/100042948; CD1263-40Q/100042949; CD1357-40C/100080365, 100080377, 100083441; CD1357-40Q/100080389, 100080390, 100083388; CD1359-40/100078740, 100083267, 100096839; CD1359-40C/100078500, 100078969, 100079372, 100079373,

St Jude Medical Inc.

FDA Devices Moderate Jul 4, 2018

Teleflex MEDICAL Pilling(R) UNIVERSAL SHEARS 7 1/2", REF 142542 Product Usage: general surgical scissors

Teleflex Medical Europe Ltd

FDA Devices Moderate Jul 4, 2018

Unify Quadra, Sterile EO, Model #/ Part #: CD3249-40/100036404, 100038435, CD3249-40Q/100036407, 100038436, CD3251-40/100036405, 100038095, 100038226, 100038437, 100038451, 100072563, CD3251-40Q/100036408, 100038214, 100038230, 100038407, 100038442, 100072564, CD3255-40/100038224, CD3255-40Q/100036514

St Jude Medical Inc.

FDA Devices Moderate Jul 4, 2018

Quadra Assura MP, Sterile EO, Model #/ Part #: CD3269-40/100043177; CD3269-40Q/100043178; CD3271-40/100043130; CD3271-40Q/100043191; CD3369-40C/100080339, 100080478; CD3369-40Q/100080439, 100080476, 100105528; CD3371-40/100078814, 100079232, 100079513; CD3371-40C/100078639, 100079231, 100079478, 100105493, 100105494; CD3371-40Q/100078815,100079282, 100079479, 100138237; CD3371-40QC/100078640, 100079165, 100079506, 100079541, 100105505, 100105506, 100138173, 100138179, 1001382

St Jude Medical Inc.

FDA Devices Moderate Jul 4, 2018

Safe N Simple No-Sting Skin Barrier Film, Ostomy Skin Barrier Wipe, SNS00807

Safe N Simple, LLC

FDA Devices Moderate Jul 4, 2018

ARTIS Pheno Interventional Fluoroscopic X-Ray System, Model 10849000

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 4, 2018

Artis zee biplane MN, Material no. 10094143, for angiography and whole body radiographic/fluoroscopic procedures.

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 4, 2018

Artis zeego, Material no. 10280959 , for angiography and whole body radiographic/fluoroscopic procedures.

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 4, 2018

ImagePilot, Model No. D9MA

Konica Minolta Medical Imaging USA, Inc.

FDA Devices Moderate Jul 4, 2018

Promote, Sterile EO, Model #/ Part #: 3207-30/60010740-207, 60010740-407; 3207-36/60010743-207, 60010743-407; 3213-36/50022126-001, 60013879-307, 60013879-407, 60013879-707; CD3211-36/100006984,100012548, 100012550, 100016680, 100031621, 100035618, 100035619, 100042487, 100047194; CD3211-36Q/100004091, 100004093,100019784, 100035620, 100042486, 100047054; CD3215-36/100006995, 100010246, 100010247, 100010249, 100010250, 100012569, 100012570, 100034981, 100046577, 100046802, 60019065;

St Jude Medical Inc.

FDA Devices Moderate Jul 4, 2018

Ellipse, Sterile EO, Model #/ Part #: CD1275-36/100116115; CD1275-36Q/100116116; CD1277-36/100048388, 100048391, 100060126, 100116208, 10011636; CD1277-36Q/100048374, 100048394, 100060198, 100098497, 100116268, 100116345; CD1293-36Q/100057838; CD1309-36/100057717; CD1309-36Q/100057718; CD1311-36/100057802, 100060153; CD1311-36Q/100057803, 100060174, 100116264; CD1377-36/100078796, 100079180, 100096847; CD1377-36C/100078612, 100079197, 100079368, 100116120, 100116407, 1001164

St Jude Medical Inc.

FDA Devices Moderate Jul 4, 2018

Diagnostic Ultrasound System, Aplio I-series. Labeled as i700, i800, i900 The power supply unit may be damaged and may fail to start up when the power plug is inserted into a power outlet while the main power switch on the rear of the system is set to ON.

Toshiba American Medical Systems Inc

FDA Devices Moderate Jul 4, 2018

Current, Sterile EO, Model #/ Part #: 1207-30/50020236-001, 60010739-207, 60010739-407; 1207-36/50020237-001, 60010742-207, 60010742-307, 60010742-407, 60010742-707; 2207-30/ 50020238-001, 60010738-207; 2207-36/ 50020239-001, 60010741-207, 60010741-307, 60010741-407, 60010741-707; CD1211-36/100006983, 100012542, 100016679, 100031495, 100035634, 100035635, 100042587, 100047090; CD1211-36Q/100004079, 100004081, 100019783, 100035607, 100042591, 100047191; CD1215-36/100006990, 100010230,

St Jude Medical Inc.

FDA Devices Moderate Jul 4, 2018

Vanguard Complete Knee System; E1 Vanguard PS Tibial Bearing; Model Numbers EP-183664, EP-183642 Product Usage: The product is intended for use in knee joint replacement arthroplasties.

Zimmer Biomet, Inc.

FDA Devices Moderate Jul 4, 2018

The Proton Therapy System - Proteus 235 (brand names: Proteus Plus and Proteus ONE) Proteus 235, Beam Management System (PBS)

Ion Beam Applications S.A.

FDA Devices Moderate Jul 4, 2018

HLD Systems 600 Series Washer/Pasteurizer, UDI (01) 0085249007009 (11) 160929 (21) 61160; Model 610HT, 115V & Model 610HT, 230V Product Usage: Clean and thermally disinfect medical devices using full immersion pasteurization

Cenorin, LLC

FDA Devices Moderate Jul 4, 2018

OmniDiagnost-Eleva X-ray system Angiographic and Diagnostic, Product Nos. 708026, 708027, 708028

Philips Medical Systems Nederlands

FDA Devices Moderate Jul 4, 2018

Artis zee MP, Material no. 10094139, for angiography and whole body radiographic/fluoroscopic procedures.

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 4, 2018

Artis zee biplane, Material no. 10094141, for angiography and whole body radiographic/fluoroscopic procedures.

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Jul 4, 2018

Single Chamber Temporary External Pacemaker, Model 53401

Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

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: USDA FSIS Recalls - calendar-year meat, poultry, and processed egg product recall filings
  • Source: CPSC + NHTSA - consumer product and vehicle recall feeds for 2018

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 2018 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.