PlainRecalls

2017 Recalls

7,480 recalls · Page 79 of 150

2017 Recall Year Insight

Federal agencies issued 7,480 product recalls indexed by PlainRecalls in calendar year 2017. That represents about 8.91% of the 83,949 total recalls we track from 1995 through the present, and averages roughly 20.5 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 150 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 2017.

On this page of 50 records, severity classification shows 1 critical, 42 moderate, and 7 lower-severity recalls. The page references 29 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 (41), FDA Drug (6), CPSC (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 2017 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 Drug Moderate Jun 7, 2017

morphine sulfate in 0.9% Sodium Chloride injectable, 1 mg per mL, Total Volume 100 mL, Single Dose Container bag, (Total morphine Dose 100 mg/ 100mL)…

SCA Pharmaceuticals

FDA Drug Moderate Jun 7, 2017

ceFAZolin sodium added to 100 mL 0.9% Sodium Chloride injectable, 3g, Total Approximate Volume 115 mL, Single Dose Container bag, Preservative Free,…

SCA Pharmaceuticals

FDA Drug Low Jun 7, 2017

Amoxicillin and Clavulanate Potassium Tablets, USP, 500 mg/125 mg, in 20 count bottles, Rx Only, Manufactured in Austria by Sandoz Gmbh for Sandoz In…

Sandoz Inc

FDA Drug Moderate Jun 7, 2017

PHENYLephrine HCL in 0.9% Sodium Chloride injectable, 10 mg (Final Concentration = 0.1 mg per mL) Total Volume 100 mL, Single Dose Container bag, Pre…

SCA Pharmaceuticals

FDA Drug Moderate Jun 7, 2017

Saphris 10 mg (asenapine) sublingual tablets, 6x10 count blister packs, Rx only, Black Cherry Flavor, Manufactured by: Catalent UK Swindon, Zydis Ltd…

Forest Laboratories, LLC

FDA Drug Moderate Jun 7, 2017

fentaNYL (as citrate) in 100mL 0.9% Sodium Chloride injectable,20 mcg per mL, Single Dose Container bag, (Total fentanyl Dose 2,000 mcg/100 mL) Prese…

SCA Pharmaceuticals

FDA Devices Moderate Jun 7, 2017

NMT Patient Cable (989803174581) in use with lntelliVue NMT Module (Part# 865383)

Philips Electronics North America Corporation

FDA Devices Moderate Jun 7, 2017

The Acumed Slide-Loc Anatomic Radial Head System is intended for use by surgeons with orthopedic training. The device is to be implanted by the surg…

Acumed LLC

FDA Devices Moderate Jun 7, 2017

HHV-8 (13810); 1.0 ml catalog number 265M-16; 7.0 ml catalog number-265M-18; Microbiology - Analyte Specific Reagent In vitro diagnostic use - …

Cell Marque Corporation

FDA Devices Moderate Jun 7, 2017

H. pylori (polyclonal} 1.0 mL Catalog number 215A-76; Hematology - Analyte Specific Reagent In vitro diagnostic use - Analyte Specific Reagent

Cell Marque Corporation

FDA Devices Low Jun 7, 2017

Beef Extract Powder, Acumedia PN 7228 Product Usage: Beef Extract Powder is prepared and standardized for use in microbiological culture media, w…

Acumedia Manufacturers, Inc.

FDA Devices Low Jun 7, 2017

Liquid Urine Control Level 3 For Professional Use in the quality control monitoring of In-Vitro Diagnostic Urinary Clinical Assays on a range of c…

Randox Laboratories

FDA Devices Moderate Jun 7, 2017

Pausch Uroview FD fluoroscopic X-ray system UDI number (01)04260491620040 Primarily for urological applications (functional X-ray diagnostics, endo…

Hans Pausch Rontgengeratebau Gmbh

FDA Devices Low Jun 7, 2017

Sabouraud Dextrose Agar w /Lecithin and Tween 20 Acumedia PN 91081 Product Usage: Used for the isolation of fungi from surfaces sanitized with q…

Acumedia Manufacturers, Inc.

FDA Devices Moderate Jun 7, 2017

Dolphin Inflation Device, REF 0185NA. Rx only, Sterilized using Ethylene Oxide. DOLPHIN is a single-use, sterile inflation device used in cardi…

Vascular Solutions, Inc.

FDA Devices Moderate Jun 7, 2017

AbbVie PEG, PEG Kit 15FR, FOR ENTERAL USE ONLY, STERILE, Rx Only.

AbbVie Inc.

FDA Devices Moderate Jun 7, 2017

Varicella Zoster Virus 7.0 ml catalog number 364M-18 Microbiology - Analyte Specific Reagent In vitro diagnostic use - Analyte Specific Reagent

Cell Marque Corporation

FDA Devices Moderate Jun 7, 2017

Exact Sciences Sample Mixer 2. For In Vitro Diagnostic Use. The Exact Sciences Sample Mixer 2 is intended for mixing stool samples in a Sample Cont…

Exact Sciences Corporation

FDA Devices Moderate Jun 7, 2017

AbbVie PEG, PEG Kit 20FR, FOR ENTERAL USE ONLY, STERILE, Rx Only.

AbbVie Inc.

FDA Devices Low Jun 7, 2017

Nutrient Gelatin, Acumedia Part Number 7471 A Product Usage: Nutrient Gelatin is used for the differentiation of microorganisms on the basis of g…

Acumedia Manufacturers, Inc.

FDA Devices Moderate Jun 7, 2017

Assist Bed Rail - 6632

Invacare Corporation

FDA Devices Moderate Jun 7, 2017

Herpes Simplex Virus I; 7.0 mL Catalog number 361A-18. Microbiology - Analyte Specific Reagent In vitro diagnostic use - Analyte Specific Reagent

Cell Marque Corporation

FDA Devices Moderate Jun 7, 2017

Endopath ETS-FLEX Endoscopic Articulating Linear Cutter, VASCULAR/THIN 35MM

Ethicon Endo-Surgery Inc

FDA Devices Low Jun 7, 2017

AIA-PACK TPOAb CONTROL SET

Tosoh Bioscience, Inc.

FDA Devices Moderate Jun 7, 2017

1000 ml Canister (with Gel) for InfoV.A.C. and V.A.C.ULTA Therapy Systems (Part Number M8275093/5). The InfoV.A.C. and V.A.C.ULTA Negative Pressur…

KCI USA, INC.

FDA Devices Moderate Jun 7, 2017

AbbVie PEG, PEG Kit 15FR, FOR ENTERAL USE ONLY, STERILE, Rx Only.

AbbVie Inc.

FDA Devices Moderate Jun 7, 2017

Her2/Neu (EP3); 0.5 mL Catalog number 237R-25; 1.0 mL Catalog number 237R-26; 7.0 mL Catalog number 237R-28. Immunology - Analyte Specific Reag…

Cell Marque Corporation

FDA Devices Moderate Jun 7, 2017

Herpes Simplex Virus II 0.5 ml catalog number 362A-15 7.0 mL Catalog number362A-18 . Microbiology - Analyte Specific Reagent In vitro diagnosti…

Cell Marque Corporation

FDA Devices Moderate Jun 7, 2017

Angio WorkStation (XIDF-AWS801) used in conjunction with your Infinix System (INFX-8000V;INFX-8000C;INFX-8000F

Toshiba American Medical Systems Inc

FDA Devices Moderate Jun 7, 2017

AFFIXUS Hip Fracture Nail Product Usage: The Hip Fracture Nail System is intended to treat stable and unstable proximal fractures of the femur in…

Zimmer Biomet, Inc.

FDA Devices Moderate Jun 7, 2017

Table Patient Step on RFX/SFX, Legacy, and Precision 500D systems

GE Healthcare, LLC

FDA Devices Moderate Jun 7, 2017

Cardinal, Digital Bariatric Scale 1) model 6876, Cap 600 and 2) model 6868 Cap 1000

Cardinal Scale Mfg Co

FDA Devices Moderate Jun 7, 2017

Modular Hybrid Glenoid Base Large for the Comprehensive Shoulder System, The product is placed into an AlOx coated PET pouch and vacuum sealed with a…

Zimmer Biomet, Inc.

FDA Devices Low Jun 7, 2017

AIA-PACK TgAb CONTROL SET

Tosoh Bioscience, Inc.

FDA Devices Moderate Jun 7, 2017

Elecsys PreciControl Varia 3

Roche Diagnostics Corporation

FDA Devices Moderate Jun 7, 2017

Adenovirus (20/11 & 2/6); 0.5 mL Catalog # 212M-15; and 7.0 mL Catalog number 212M-18 Microbiology - Analyte Specific Reagent In vitro diagno…

Cell Marque Corporation

FDA Devices Moderate Jun 7, 2017

CD117, c-kit (YR145) 1.0 ml catalog number 117R-16 7.0 ml catalog number-18 Microbiology - Analyte Specific Reagent In vitro diagnostic use - A…

Cell Marque Corporation

FDA Devices Moderate Jun 7, 2017

Reusable instruments in the Knee, Hip, Trauma, and Extremities segments.

Zimmer Biomet, Inc.

FDA Devices Moderate Jun 7, 2017

Arrow(R) VPS(R) Access Kit for use with 4 and 5 Fr. Peripherally Inserted Central Venous Catheters

Arrow International Inc

FDA Devices Moderate Jun 7, 2017

Pointe Scientific Lactate Dehydrogenase (Liquid) Reagent Set Model Number(s): L7572. For the in vitro quantitative kinetic determination of lact…

Medtest Holdings, Inc.

FDA Devices Moderate Jun 7, 2017

SHBG IMMULITE 2000/IMMULITE 2000 XPi For the in vitro diagnostic use with the IMMULITE 2000 Systems Analyzers-For the quantitative measurement of SH…

Siemens Healthcare Diagnostics, Inc.

FDA Devices Critical Jun 7, 2017

Absorb Bioresorbable Vascular Scaffold (BVS) system (Australia). The Absorb BVS is a temporary scaffold indicated for improving coronary luminal dia…

Abbott Vascular

FDA Devices Moderate Jun 7, 2017

Draco Enzymatic Deep-Cleaning Pad with Enzymatic Detergent Catalogue Number: HY0305Z

Madison Polymeric Engineering

FDA Devices Moderate Jun 7, 2017

Estrogen Receptor (SP1) 7.0 mL Catalog number 249R-18; Hematology - Analyte Specific Reagent In vitro diagnostic use - Analyte Specific Reagent

Cell Marque Corporation

FDA Devices Moderate Jun 7, 2017

SV40 (MRQ-4) 0.5 ml catalog number 351 M-15. Microbiology - Analyte Specific Reagent In vitro diagnostic use - Analyte Specific Reagent

Cell Marque Corporation

FDA Devices Moderate Jun 7, 2017

Estrogen Receptor (EP1) 7.0 mL Catalog number 249R-28; 1.0 mL Catalog number 249R-16 Microbiology - Analyte Specific Reagent In vitro diagno…

Cell Marque Corporation

FDA Devices Moderate Jun 7, 2017

Her2/Neu (c-erbB-2) (CB-1 1); 7.0 mL Catalog number 237M-18. In vitro diagnostic use - Analyte Specific Reagent Immunology - Analyte Specific Re…

Cell Marque Corporation

CPSC Moderate Jun 7, 2017

Lithonia Lighting Recalls to Repair Ceiling Light Fixtures Due to Impact Hazard

Lithonia Lighting, a division of Acuity Brands Lighting Inc., of Conyers, Ga.

CPSC Moderate Jun 7, 2017

Madison Mill Recalls Safety Gates Due to Entrapment and Strangulation Hazards

Madison Mill Inc., of Ashland City, Tenn.

CPSC Moderate Jun 7, 2017

Nidec Motor Recalls Swimming Pool Motors Due to Electrical Shock Hazard

Nidec Motor Corp., of St. Louis, Mo.

Nearby Recall Years

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

Compare 2017 with 2016 →

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 2017