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 10 critical, 39 moderate, and 1 lower-severity recalls. The page references 34 distinct recalling firms operating in 7 distinct product categories, with 45 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (33), CPSC (6), NHTSA (5), 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 Devices Moderate Feb 21, 2018

PENCAN Spinal Anesthesia Tray. Product Catalog Number: 560590. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.

B. Braun Medical, Inc.

FDA Devices Moderate Feb 21, 2018

3M Bair Hugger(M) Normothermia System, Sterile Full Access Underbody, Model 63700 The 3M Bair Hugger Temperature Management System is intended to prevent and treat hypothermia. In addition, the temperature management system can be used to provide patient thermal comfort when conditions exist that may cause patients to become too warm or too cold. The temperature management system can be used with adult and pediatric patients.

3M Company - Health Care Business

FDA Devices Moderate Feb 21, 2018

A.T.S. 2200TS Tourniquet Systems, Personalized Pressure. Zimmer Surgical, Inc. Dover, OH 44622 Intended to be used by qualified professionals to temporarily occlude blood flow in a patient's extremities during surgical procedures on those extremities.

Zimmer Surgical Inc

FDA Devices Moderate Feb 21, 2018

Ingenuity TF PET/CT (model 882442) running software version 4.0.2 This device is a diagnostic imaging system that combines Positron Emission Tomography (PET) and X-ray Computed Tomography (CT) systems. The CT subsystem produces cross-sectional images of the body by computer reconstruction of x-ray transmission data. The PET subsystem produces images of the distribution of PET radiopharmaceuticals in the patient body (specific radiopharmaceuticals are used for whole body, brain, heart and ot

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Feb 21, 2018

Perifix Single Dose Epidural Anesthesia Tray. Product Catalog Number: 332252. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.

B. Braun Medical, Inc.

FDA Devices Low Feb 21, 2018

Purely Yours Breast Pump. Model 17070PMW and Model 17070ACA. Intended to express and collect the mother s milk from the breasts of a nursing woman for the purpose of feeding the collected milk to a baby.

AMEDA, INC.

FDA Devices Moderate Feb 21, 2018

Perifix FX Epidural Anesthesia Tray. Product Catalog Numbers: 551993, 552051, 552083, 552119, 555569. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.

B. Braun Medical, Inc.

FDA Devices Moderate Feb 21, 2018

NS357R Vega PS Tibia Trial/Preparation Plateau size T4 (Component of the Vega Knee System Set #ST0468) The affected part is provided in the Vega Knee System Set #ST0468. The Vega Knee System is used for reconstruction of the diseased knee joint.

Aesculap Implant Systems LLC

FDA Devices Moderate Feb 21, 2018

Norian Drillable Inject

Synthes USA

FDA Devices Moderate Feb 21, 2018

CORAIL COXA VARA HIGH OFFSET STEM Collared Size 9

DePuy Orthopaedics, Inc.

FDA Devices Moderate Feb 21, 2018

Central Venous Catheter Set Triple Lumen Polyurethane, Catalog Identifier: C-UTLM-501J Product Usage: The central venous catheter is designed for treatment of critically ill patients and is suggested for: 1. Continuous or intermittent drug infusions; 2. Central venous blood pressure monitoring (CVP); 3. Acute hyperalimentation; 4. Blood sampling; 5. Delivery of whole blood or blood products; 6. Simultaneous, separate infusion of drugs

Cook Inc.

FDA Devices Moderate Feb 21, 2018

ArrowADVANTAGE 5 Pressure Injectable Peripherally Inserted Central Catheter (PICC). Product Codes: PR-35041-HPHNM and CDA-35041-HPK1A.

Arrow International Inc

FDA Devices Moderate Feb 21, 2018

A.T.S. 4000TS Tourniquet Systems, Personalized Pressure. Intended to be used by qualified professionals to temporarily occlude blood flow in a patient's extremities during surgical procedures on those extremities. .

Zimmer Surgical Inc

FDA Devices Moderate Feb 21, 2018

Central Venous Catheter Tray Triple Lumen Polyurethane, Catalog Identifier: C-UTLMYJ-501J Product Usage: The central venous catheter is designed for treatment of critically ill patients and is suggested for: 1. Continuous or intermittent drug infusions; 2. Central venous blood pressure monitoring (CVP); 3. Acute hyperalimentation; 4. Blood sampling; 5. Delivery of whole blood or blood products; 6. Simultaneous, separate infusion of drugs

Cook Inc.

FDA Devices Moderate Feb 21, 2018

Carestation 620 A2, Carestation 650 A2, and Carestation 650c A2

GE Medical Systems China Co., Ltd.

FDA Devices Moderate Feb 21, 2018

Artis oneFloor-mounted system for uncompromised imaging; Artis one, Interventional fluoroscopic x-ray system, Artis one is an angiography system developed for diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. X-ray generator POLYDOROS A100 Plus

Siemens Medical Solutions USA, INC

FDA Devices Moderate Feb 21, 2018

BARD(R) CRITICORE(R) MONITOR, Model: 000002N Series The CritiCore(R) Automated Urine Output and Temperature Monitor is indicated to monitor urine output and core bladder temperature.

C.R. Bard, Inc.

FDA Devices Moderate Feb 21, 2018

Xpert CT/NG Catalog GXCT/NG-120 Batch 1000049568, Catalog GXCT/NG-10 Batch 1000053075, Catalog GXCT/NG-10 Batch 1000056156 and Catalog GXCT/NG-10 Batch 1000056157. Is a qualitative in vitro real-time PCR test.

Cepheid

FDA Devices Moderate Feb 21, 2018

AGC 2000 LP Patella, labeled as AGC Porous Patellar Med, Model Number 150804. Product Usage: For use in Total Knee Arthroplasty.

Zimmer Biomet, Inc.

FDA Devices Moderate Feb 21, 2018

ELAN 4 Drill: ELAN 4 1-RING TWIST DRILL D1.5 ELAN 4 1-RING TWIST DRILL D2.0 ELAN 4 2-RING TWIST DRILL D1,0/4,0MM ELAN 4 2-RING TWIST DRILL D1,1/4,0MM ELAN 4 2-RING TWIST DRILL D1,2/4,0MM ELAN 4 2-RING TWIST DRILL D1,5/4,0MM ELAN 4 2-RING TWIST DRILL D1,5 ELAN 4 2-RING TWIST DRILL D2,0 ELAN 4 2-RING WIRE PASS DRILL D1.0 ELAN 4 2-RING WIRE PASS DRILL D1.5 ELAN 4 2-RING WIRE PASS DRILL D2.0 ELAN 4 2-RING WIRE PASS DRILL D1.0 ELAN 4 2-RING WIRE PASS DRILL D1.5 ELAN 4 2-RING WIRE PASS DR

Aesculap Implant Systems LLC

FDA Devices Moderate Feb 21, 2018

Customer Epidural Anesthesia Tray. Product Catalog Number: 555234. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.

B. Braun Medical, Inc.

FDA Devices Moderate Feb 21, 2018

Pencan Spinal Needle Tray. Product Catalog Number: 333865. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.

B. Braun Medical, Inc.

FDA Devices Moderate Feb 21, 2018

Pain Management Tray. Product Catalog Number: 560602. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.

B. Braun Medical, Inc.

FDA Devices Moderate Feb 21, 2018

Exactech GPS Total Shoulder Application 3.2mm Vix Bit Orthopedic surgical tool

Exactech, Inc.

FDA Devices Moderate Feb 21, 2018

BlockAid Cut Resistant Surgical Glove Liners, combine stainless steel and synthetic fibers woven together to form a cut resistant glove material. Blockaid Cut Resistant Surgical Glove Liners are to be worn between two layers of surgical gloves. Item Number: 650126, 650127, 650128, 650129, 650130, 650131

Zimmer Biomet, Inc.

FDA Devices Moderate Feb 21, 2018

Spectrum Central Venous Catheter Tray Minocycline/Rifampin Antibiotic Impregnated, Catalog Identifiers: C-UTLMY-501J-ABRM-HC-FST and C-UTLMY-501J-ABRM-HC-IHI-FST Usage: The Spectrum Central Venous Catheter is used for the intravenous administration of nutrient fluids, chemotherapeutic agents, and other drugs for therapy, blood sampling, blood delivery, and venous pressure monitoring

Cook Inc.

FDA Devices Moderate Feb 21, 2018

Hemotherm¿ Dual Reservoir Cooler/Heater System Models 400CE and 400MR Product Usage: A dual reservoir, water re-circulating device that supplies temperature controlled water to a heat exchanger. The device, in conjunction with a heat exchanger, is used to warm or cool the blood that enters and exits a blood heat exchanger for adult, pediatric or infant patients.

Cincinnati Sub-Zero Products LLC

FDA Devices Moderate Feb 21, 2018

Model #: CG8900, Medtronic Clip Gun Scalp Clip Kit (Qty 1); Model #: CG8901, Medtronic Clip Gun Scalp Clip Kit (Qty 10); Model #: CG8901A, Medtronic Clip Gun Applicator (Qty 10)

Medtronic Neurosurgery

FDA Devices Moderate Feb 21, 2018

Total Knee Replacement , Catalog/Model # TPS-111-1111, UDI: +M572TPS1111111021/$$+31712310398482- and +M572TPS1111111021/$$+31712310399917/ Intended for use as a total knee replacement in patients with knee joint pain and disability whose conditions cannot be solely addressed by the use of a prosthetic device that treats only one or two of the three knee compartments, such as a unicondylar, patellofemoral, or bicompartmental prosthesis.

ConforMIS, Inc.

FDA Devices Moderate Feb 21, 2018

Contiplex Nerve Block Tray. Product Catalog Number: 570205. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.

B. Braun Medical, Inc.

FDA Devices Moderate Feb 21, 2018

Custom Made Tracheostomy Device The CADD Administration Sets with Flow Stop are designed to be used with a variety of CADD ambulatory infusion pumps to allow fluid delivery from an IV bag.

Smiths Medical ASD, Inc.

FDA Devices Moderate Feb 21, 2018

JS Series SterilContainer S2 System

Aesculap Implant Systems LLC

FDA Devices Moderate Feb 21, 2018

Carestation 620 A1, Carestation 650 A1, and Carestation 650c A1

GE Medical Systems China Co., Ltd.

CPSC No agency class Feb 21, 2018

Cost Plus World Market Recalls Bleeding Drip Taper Candles Due to Fire Hazard

Proud Wealth International LTD, of China

CPSC No agency class Feb 21, 2018

Outdoor Gas Fire Pits Recalled Due to Burn Hazard; Sold Exclusively at Home Depot; Made by Yayi

Zhejiang Yayi Metal Technology Co., Ltd. dba Yayi, of China

USDA FSIS Critical Feb 21, 2018

A & A Finest Recalls Frozen Pork and Shrimp Dumpling Products due to Misbranding and an Undeclared Allergen

A & A Finest

USDA FSIS Critical Feb 21, 2018

Triple T Specialty Meats Inc. Recalls Chicken Salad Products Due to Possible Salmonella Contamination

CPSC No agency class Feb 20, 2018

NEMO Equipment Recalls Stargaze Recliner Chairs Due to Fall Hazard; Sold Exclusively at REI

NEMO Equipment of Dover, N.H.

CPSC No agency class Feb 20, 2018

Whirlpool Recalls KitchenAid Electric Kettles Due to Burn Hazard

Co-Win Global Ltd, of Hong Kong

NHTSA No agency class Feb 20, 2018

TOYOTA 2017: SEATS:MID/REAR ASSEMBLY

TOYOTA

NHTSA No agency class Feb 20, 2018

TOYOTA 2018: ELECTRONIC STABILITY CONTROL (ESC)

TOYOTA

USDA FSIS Critical Feb 20, 2018

Night Hawk Frozen Foods, Inc. Recalls Frozen Beef Products Due to Misbranding and Undeclared Allergens

Night Hawk Frozen Foods, Inc.

NHTSA No agency class Feb 17, 2018

HYUNDAI 2018: STEERING: STEERING WHEEL/HANDLE BAR

HYUNDAI

USDA FSIS Critical Feb 16, 2018

Pilgrim's Pride Corporation Recalls Ready-to-Eat Chicken Products due to Possible Foreign Matter Contamination

Pilgrim's Pride Corporation

CPSC No agency class Feb 15, 2018

Rural King Recalls Electric Blankets and Throws Due to Fire and Burn Hazards

CPSC No agency class Feb 15, 2018

Specialized Bicycle Components Recalls Bicycles Due to Crash Hazard

Specialized Bicycle Components Inc., of Morgan Hill, Calif.

NHTSA No agency class Feb 15, 2018

MERCEDES-BENZ 2016-2017: EQUIPMENT:OTHER:LABELS

MERCEDES-BENZ

NHTSA No agency class Feb 15, 2018

JAGUAR 2018: AIR BAGS

JAGUAR

FDA Food Moderate Feb 14, 2018

Wienke's Market Strawberry Raspberry Jam, Net Wt. 8 oz (226g), UPC 14106-00235. Refrigerate after opening. Ingredients: strawberries, raspberries, sugar, pectin.

Wienke LLC

FDA Food Critical Feb 14, 2018

Pound Cake NET WT 4OZ and 12OZ.

Productos Pacheco, Inc.

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.