PlainRecalls

2016 Recalls

8,148 recalls · Page 155 of 163

2016 Recall Year Insight

Federal agencies issued 8,148 product recalls indexed by PlainRecalls in calendar year 2016. That represents about 9.71% of the 83,949 total recalls we track from 1995 through the present, and averages roughly 22.3 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 163 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 2016.

On this page of 50 records, severity classification shows 7 critical, 42 moderate, and 1 lower-severity recalls. The page references 22 distinct recalling firms operating in 7 distinct product categories, with 42 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Drug (21), FDA Devices (11), 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 2016 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 Feb 10, 2016

INTEGRIS BV3000 MONO; Model Number: 72241 The Philips INTEGRIS 3000 I 5000 system is intended for interventional and diagnostic vascular and neuro…

Philips Electronics North America Corporation

FDA Devices Moderate Feb 10, 2016

Allura Xper FD20 OR Table; Model Numbers: 722035 722023 Dedicated vascular and neurovascular imaging applications, including diagnostic and interv…

Philips Electronics North America Corporation

FDA Devices Moderate Feb 10, 2016

DS/US Proton Feature with Pinnacle3 Software Version 10.0.0 and 14.0.0 Radiation Therapy Planning System Model #459800200621

Philips Medical Systems

FDA Devices Moderate Feb 10, 2016

API ZYM Bx2 (Ref 70493) Product Usage: ZYM B reagent is an additional test used for revealing the results of some miniaturized biochemical test i…

BioMerieux SA

FDA Devices Moderate Feb 10, 2016

MediChoice Cohesive Bandages, One (1) roll of cohesive bandage per bag, thirty-six (36) bags per case [all model numbers have equivalent packaging] …

Owens & Minor Distribution, Inc.

FDA Devices Moderate Feb 10, 2016

Allura Xper FD20/15; Model Numbers: 722058 Dedicated vascular and neurovascular imaging applications, including diagnostic and interventional proc…

Philips Electronics North America Corporation

FDA Devices Moderate Feb 10, 2016

Allura Xper FD20/20; Model Number: 722038 Dedicated vascular and neurovascular imaging applications, including diagnostic and interventional proc…

Philips Electronics North America Corporation

FDA Devices Moderate Feb 10, 2016

ABX PENTRA Enzymatic Creatinine CP ref. A11A01907 reagent is intended for the quantitative in vitro diagnostic determination of creatinine in human s…

Horiba Instruments Inc

FDA Devices Moderate Feb 10, 2016

ADVIA Centaur PSA Assay; Catalog Number: 06574155/SMN 10310292 (100 test kit) and Catalog Number: 02676506/SMN 10310293 (500 test kit) Product Usa…

Siemens Healthcare Diagnostics, Inc

FDA Devices Moderate Feb 10, 2016

Denali Filter-Jugular/Subclavian DL950J Denali Filter-Femoral Delivery DL950F. Intravascular filters.

Bard Peripheral Vascular Inc

FDA Devices Moderate Feb 10, 2016

UNIQ FD OR table; Model Number 722035 The Philips UNIQ is intended for use on human patients to perform: " Vascular, cardiovascular and neurovascu…

Philips Electronics North America Corporation

CPSC Moderate Feb 10, 2016

Arctic Cat Recalls Snowmobiles Due to Crash, Injury Hazards (Recall Alert)

Arctic Cat Inc., of Thief River Falls, Minn.

CPSC Moderate Feb 10, 2016

Pier 1 Imports Recalls Swivel Dining Chairs Due to Fall Hazard

NHTSA Critical Feb 10, 2016

AUDI 2006-2013: AIR BAGS:FRONTAL:DRIVER SIDE:INFLATOR MODULE

AUDI

NHTSA Critical Feb 10, 2016

AUDI 2009-2012: AIR BAGS:FRONTAL:DRIVER SIDE:INFLATOR MODULE

AUDI

NHTSA Critical Feb 10, 2016

DODGE,FREIGHTLINER,MERCEDES-BENZ 2007-2014: AIR BAGS:FRONTAL:DRIVER SIDE:INFLATOR MODULE

DODGE,FREIGHTLINER,MERCEDES-BENZ

CPSC Moderate Feb 9, 2016

Classic Characters Recalls Infant Booties Due to Choking Hazard; Sold Exclusively at Cracker Barrel Old Country Store

CPSC Moderate Feb 9, 2016

IKEA Recalls Ceiling Lamps Due to Laceration Hazard

NHTSA Critical Feb 9, 2016

HONDA 2016: ENGINE AND ENGINE COOLING:ENGINE

HONDA

NHTSA Critical Feb 5, 2016

BMW 2006-2015: AIR BAGS:FRONTAL:DRIVER SIDE:INFLATOR MODULE

BMW

NHTSA Critical Feb 5, 2016

KIA 2011: POWER TRAIN:AUTOMATIC TRANSMISSION:COOLING UNIT AND LINES

KIA

NHTSA Critical Feb 5, 2016

CHEVROLET,GMC 2015-2016: SERVICE BRAKES, HYDRAULIC:PEDALS AND LINKAGES

CHEVROLET,GMC

NHTSA Moderate Feb 5, 2016

LEXUS 2003-2006: AIR BAGS:SIDE/WINDOW

LEXUS

CPSC Moderate Feb 4, 2016

CE North America Recalls Fan Heaters Due to Fire Hazard; Sold Exclusively at Bed Bath & Beyond

CPSC Moderate Feb 4, 2016

Dollar General Recalls Construction Truck Toy Vehicles Due to Fire and Burn Hazards; Sold Exclusively at Dollar General

Dollar General Corp., of Goodlettsville, Tenn.

CPSC Moderate Feb 4, 2016

Head USA Recalls Ski and Snowboard Helmets Due to Head Injury Hazard

Head USA, of Boulder, Colo.

CPSC Moderate Feb 4, 2016

KHS America Recalls Children's Musical Instrument Due to Violation of Lead Paint Standard

CPSC Moderate Feb 4, 2016

Wedgwood Decorative Baby Rattles Recalled by WWRD Due to Choking Hazard

FDA Food Moderate Feb 3, 2016

Mandarin Oranges (In Light Syrup), Net Wt. 8oz (227g), Case UPC#: 100-49022-80895-6, Product UPC#: 0-49022-80895-9

Milky Way Intl Trading Corp

FDA Drug Moderate Feb 3, 2016

Provocholine Pre-diluted Set II in 0.9% Sodium Chloride, 0.0625 mg/mL, 3 mL in 5 mL Syr, injectable packed in syringes, Rx only, PHARMAKON Pharmaceut…

Pharmakon Pharmaceuticals

FDA Drug Moderate Feb 3, 2016

Dextrose-NaCl (D5-1/2NS) in NS, Packaged in a) 1700ML Homepumps, b) 1800ML Homepumps, and c) 1920ML Homepumps, Rx Only. SENTARA HOME HEALTH SENTARA …

Sentara Enterprises

FDA Drug Moderate Feb 3, 2016

Guaifenesin DM Cherry liquid (guaifenesin 100 mg/5 mL and Dextromethorphan HBr 5 mg/5 mL), packaged in 4oz. bottles, co-packaged with a dosing cup in…

Perrigo Company PLC

FDA Drug Moderate Feb 3, 2016

Ketamine 50 mg/mL, injectable packed in syringes, Total dosage 50 mg/ 1mL, Rx only, PHARMAKON Pharmaceuticals, Inc.

Pharmakon Pharmaceuticals

FDA Drug Moderate Feb 3, 2016

Lactated Ringers, Packaged in a) 1500ML Homepumps, b) 2800ML Homepumps, and c) 3600ML Homepumps, Rx Only. SENTARA HOME HEALTH SENTARA RX, 535 Indepen…

Sentara Enterprises

FDA Drug Moderate Feb 3, 2016

Ephedrine Sulfate 5 mg/mL in 0.9% Sodium Chloride, injectable packed in syringes, Total dosage 25 mg/ 5mL, Rx only, PHARMAKON Pharmaceuticals, Inc.

Pharmakon Pharmaceuticals

FDA Drug Moderate Feb 3, 2016

HYDROMORPHONE HCL, Packaged as a) 2.5MG in 1ML Syringes, b) 150MG in 75ML Homepumps, c) 125MG in 125ML Homepumps, d) 250MG in 125ML Homepumps, e) 135…

Sentara Enterprises

FDA Drug Moderate Feb 3, 2016

Dextrose-5% Lactated Ringers, Packaged in 3000ML Homepumps, Rx Only. SENTARA HOME HEALTH SENTARA RX, 535 Independence Pkwy ste.300, Chesapeake, VA 23…

Sentara Enterprises

FDA Drug Moderate Feb 3, 2016

CLINDAMYCIN 120MG in NS, Package in 20ML Homepumps, Rx Only. SENTARA HOME HEALTH SENTARA RX, 535 Independence Pkwy ste.300, Chesapeake, VA 23320-5176.

Sentara Enterprises

FDA Drug Moderate Feb 3, 2016

Phenylephrine (PF) 100 mcg/mL in 0.9% Sodium Chloride, injectable packed in syringes, Total dosage 500 mcg/ 5mL, Rx only, PHARMAKON Pharmaceuticals, …

Pharmakon Pharmaceuticals

FDA Drug Low Feb 3, 2016

Cyclopentolate Hydrochloride Ophthalmic Solution USP, 1%, Packaged in a) 2 mL Bottles (NDC: 24208-735-01) and b) 15 mL Bottles (NDC: 24208-735-05), R…

Bausch & Lomb, Inc.

FDA Drug Moderate Feb 3, 2016

Ketamine 100 mg/mL, injectable packed in syringes, Total dosage 100 mg/ 1mL, Rx only, PHARMAKON Pharmaceuticals, Inc.

Pharmakon Pharmaceuticals

FDA Drug Moderate Feb 3, 2016

AZACTAM (aztreonam) 2GM in NS, Packaged in 100ML Homepumps, Rx Only. SENTARA HOME HEALTH SENTARA RX, 535 Independence Pkwy ste.300, Chesapeake, VA 23…

Sentara Enterprises

FDA Drug Moderate Feb 3, 2016

Midazolam (PF) 0.1 mg/mL in 0.9% Sodium Chloride, injectable packed in syringes, Total dosage 0.2 mg/ 2mL, Rx only, PHARMAKON Pharmaceuticals, Inc.

Pharmakon Pharmaceuticals

FDA Drug Moderate Feb 3, 2016

CEFAZOLIN, Packaged as a) 625MG in 6.2ML Syringes, b) 2GM in 20ML Syringes, c) 1GM in 50ML Homepumps, d) 2GM in 100ML Homepumps, and e) 12GM in 600ML…

Sentara Enterprises

FDA Drug Moderate Feb 3, 2016

Milrinone in 0.45% NS, Packaged as a) 52MG in 65ML Homepumps, b) 80MG in 100ML Homepumps, c) 92MG in 115ML Homepumps, d) 104MG in 130ML Homepumps, e)…

Sentara Enterprises

FDA Drug Moderate Feb 3, 2016

ASCORBIC ACID 500MG/Syringe, Packaged in 1ML Syringes, Rx Only. SENTARA HOME HEALTH SENTARA RX, 535 Independence Pkwy ste.300, Chesapeake, VA 23320-5…

Sentara Enterprises

FDA Drug Moderate Feb 3, 2016

PENICILLIN in D5W, Packaged as a)36MU in 360ML Homepumps and b) 51MU in 510ML Homepumps, Rx Only. SENTARA HOME HEALTH SENTARA RX, 535 Independence Pk…

Sentara Enterprises

FDA Drug Moderate Feb 3, 2016

Invanz (ertapenem) Injection Recon Soln in NS, Packaged as a) 500MG in 50ML Homepumps and b) 1 GM in 100ML Homepumps, Rx Only. SENTARA HOME HEALTH SE…

Sentara Enterprises

FDA Drug Moderate Feb 3, 2016

Solu-Cortef (hydrocortisone) 1MG in NS, Packaged in 0.1ML Syringe, Rx Only. SENTARA HOME HEALTH SENTARA RX, 535 Independence Pkwy ste.300, Chesapeake…

Sentara Enterprises

FDA Drug Moderate Feb 3, 2016

Nafcillin 2GM in NS, Packaged in 50ML Homepumps, Rx Only. SENTARA HOME HEALTH SENTARA RX, 535 Independence Pkwy ste.300, Chesapeake, VA 23320-5176.

Sentara Enterprises

Nearby Recall Years

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

Compare 2016 with 2015 →

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 2016