PlainRecalls

2017 Recalls

7,480 recalls · Page 126 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 5 critical, 42 moderate, and 3 lower-severity recalls. The page references 32 distinct recalling firms operating in 4 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (39), FDA Drug (7), FDA Food (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 Food Moderate Feb 22, 2017

Joe Chips Retro Potato Chips Sour Cream & Toasted Onion Distributed by: The Joe Tea Company, Upper Montclair, NJ 07043-0255 (973)744-7502 Net Wt. …

The Two Little Guys Company

FDA Food Moderate Feb 22, 2017

Crystal Geyser Sparkling Mineral Water, Original; 18 oz. (53 ml) plastic bottles sold in 28 pack wrapped tray. UPC codes: Bottle Label  6 54871…

Crystal Geyser Water Company

FDA Food Critical Feb 22, 2017

Whole Foods Market, TART FRENCH APPLE SMALL

Whole Foods Market Brand 365, Llc

FDA Drug Moderate Feb 22, 2017

Mimvey Lo (estradiol and norethindrone acetate tablets USP), 0.5 mg/0.1 mg, 28 tablets per blister card (NDC 0093-5454-18), packaged in 3 blister car…

Teva Pharmaceuticals USA

FDA Drug Low Feb 22, 2017

Taclonex (calcipotriene and betamethasone dipropionate) Topical Suspension, 0.005%/0.064%, packaged in (a) 60 g (NDC 50222-501-06), and (b)120 g (5…

LEO PHARMA INC

FDA Drug Critical Feb 22, 2017

SLIMFIT X capsules, packaged in a 60-cont bottle

Jersey Shore Supplements, LLC

FDA Drug Critical Feb 22, 2017

MegaJex Herbal Supplement, Maximum Formula for Men, Fast acting, Increase Stamina, 20 capsules, MS Bionics, Gardena, CA

MS Bionic

FDA Drug Moderate Feb 22, 2017

Venlafaxine Hydrochloride extended release capsules, 37.5 mg, 30-count bottles, Rx Only, Manufactured for: Aurobindo Pharma USA, Inc. 2400 Route 130 …

Aurobindo Pharma USA Inc

FDA Drug Moderate Feb 22, 2017

Lisinopril tablets, 5 mg, 1000-count bottle, Rx only, Manufactured for Accord Healthcare, Inc., Durham, NC 27703, NDC 16729-376-17

Accord Healthcare, Inc.

FDA Drug Moderate Feb 22, 2017

Glipizide extended-release tablets, 2.5mg, 30-count bottle, Rx Only, Manufactured By Patheon Pharmaceuticals Inc Cincinnati OH 45237 USA, NDC 0591-…

Actavis Inc

FDA Devices Moderate Feb 22, 2017

Maquet Express Dry Seal Suction OCEAN DRAIN, SINGLE Reference: 2002-400 Intended Use: To evacuate air and/or fluid from the chest cavity or medias…

Atrium Medical Corporation

FDA Devices Moderate Feb 22, 2017

Atrium PVC 8 Fr Straight Thoracic Catheter Code Number: 8008

Atrium Medical Corporation

FDA Devices Moderate Feb 22, 2017

STERRAD NX Sterilization System, Product Code: 10033, 10033-002

Advanced Sterilization Products

FDA Devices Moderate Feb 22, 2017

StarClose SE Vascular Closure System, Part No. 14679-01, 14679-02. The UDI is 08717648079467. The GMDN is 47411.

Abbott Vascular

FDA Devices Moderate Feb 22, 2017

Vanguard Total Knee, PUNCH THRU TRL PLATES, 63 MM Item No: 32-487261, 67 MM Item No: 32-487262, 71 MM Item No: 32-487263, 75 MM Item No: 32-487264, a…

Zimmer Biomet, Inc.

FDA Devices Moderate Feb 22, 2017

ONCOR Avant-garde, medical charged-particle radiation therapy system Product Usage: The intended use of the SIEMENS branded PRIMUS family of lin…

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Feb 22, 2017

HARVEST NEEDLE 15GA X 2 Intended for the purpose of harvesting bone and/or bone marrow specimens

Argon Medical Devices, Inc

FDA Devices Moderate Feb 22, 2017

Maquet Ocean Water Seal Chest Drain, Single Collection w/AC Reference: 2002-100 Intended Use: To evacuate air and/or fluid from the chest cavity …

Atrium Medical Corporation

FDA Devices Moderate Feb 22, 2017

GN200 Caiman HF generators, electrosurgical, cutting & coagulation & accessories

Aesculap Implant Systems LLC

FDA Devices Critical Feb 22, 2017

Comprehensive Reverse Shoulder System Humeral Tray Model 115340

Zimmer Biomet, Inc.

FDA Devices Moderate Feb 22, 2017

ARTISTE MV System, medical charged-particle radiation therapy system Product Usage: The intended use of the SIEMENS branded PRIMUS family of lin…

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Feb 22, 2017

The Schiller PB 1000, also known as: Merge Hemo Patient Data Module (PDM), V2 model, a major component of the Merge Hemo software.

Merge Healthcare, Inc.

FDA Devices Low Feb 22, 2017

The Enzyme II Calibrator is an in vitro diagnostic product for the Alanine Aminotransferase (ALTI) on the Dimension¿ clinical chemistry system. For …

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Feb 22, 2017

LIMA Modular Revision Hip Stem Model 428-01-050_110 Product Usage: The Modular Revision Femoral hip stem is made up of a modular stem coupled wit…

Encore Medical, Lp

FDA Devices Moderate Feb 22, 2017

PRIMUS Medical charged-particle radiation therapy system Product Usage: The intended use of the SIEMENS branded PRIMUS family of linear accelera…

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Feb 22, 2017

ONCOR Impression, ONCOR Impression plus, and ONCOR Expression Medical charged-particle radiation therapy system Product Usage: The intended use o…

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Feb 22, 2017

Maquet Oasis Dry Suction Water Seal Chest Drain, Single Collection w/AC Reference: 3600-100 Intended Use: To evacuate air and/or fluid from the che…

Atrium Medical Corporation

FDA Devices Moderate Feb 22, 2017

BrightView X upgraded to XCT 882454

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Feb 22, 2017

Maquet Ocean Water Seal Chest Drain, Single Collection WAC Reference: 2002-000 Intended Use: To evacuate air and/or fluid from the chest cavity o…

Atrium Medical Corporation

FDA Devices Moderate Feb 22, 2017

Arthrex Shoulder Suspension Tower; Catalog Number: AR-1650-01 Product Usage: The Arthrex Lateral Decubitus Shoulder Positioner is intended to all…

Allen Medical Systems, Inc.

FDA Devices Moderate Feb 22, 2017

T-LOK BONE MARROW BIOPSY NEEDLE 8G x 4 EXT CAN; T-LOK BONE MARROW BIOPSY NEEDLE 11G x 4 EXT CAN Intended for the purpose of harvesting bone and/or…

Argon Medical Devices, Inc

FDA Devices Moderate Feb 22, 2017

6-hole Pubic Symphysis plate (PN 70-0451). The pelvic bone plates for the pelvic ring are a series of plates with varying lengths that function as i…

Acumed LLC

FDA Devices Low Feb 22, 2017

The Enzyme 2 Calibrator is an in vitro diagnostic product for the calibration of Alanine Aminotransferase (ALTI and ALTI) and Aspartate Aminotransfer…

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Feb 22, 2017

BD Vacutainer Buffered Sodium Citrate: (9NC) Blood Collection Tube (4.5 ml x 13 x 75 mm) Catalog Number: 369714 Product Usage: The BD Vacutaine…

Becton Dickinson & Company

FDA Devices Moderate Feb 22, 2017

Maquet Express Dry Seal Suction OASIS DRAIN, DRY PEDI W/AC Reference: 3612-100 Intended Use: To evacuate air and/or fluid from the chest cavity or…

Atrium Medical Corporation

FDA Devices Critical Feb 22, 2017

LIFEPAK 15 Monitor, Automated External Defibrillator (AED), Manual mode monitoring and therapy functions are intended for use on adult and pediatric …

Physio-Control, Inc.

FDA Devices Moderate Feb 22, 2017

Hercules 360 Universal Stabilizing Arm, top mount, 360-degree rotation, reusable stainless steel

Terumo Cardiovascular Systems Corporation

FDA Devices Moderate Feb 22, 2017

Offset Reamer Handle, T5766 Product Usage: The reamer handles are re-usable surgical instruments used in arthroplasty surgery of the hip joints, …

Greatbatch Medical

FDA Devices Moderate Feb 22, 2017

Atrium PVC 10 Fr Straight Thoracic Catheter Code Number: 8010

Atrium Medical Corporation

FDA Devices Moderate Feb 22, 2017

Maquet Express Dry Seal Suction OCEAN DRAIN, SINGLE W/S Reference: 2002-300 Intended Use: To evacuate air and/or fluid from the chest cavity or med…

Atrium Medical Corporation

FDA Devices Moderate Feb 22, 2017

BONE MARROW ASPIRATION NEEDLE 15G x 2.688 MAX and 15G x 4 MAX Intended for the purpose of harvesting bone and/or bone marrow specimens

Argon Medical Devices, Inc

FDA Devices Moderate Feb 22, 2017

Maquet Express Dry Seal Suction Chest Drain, Single Collection w/AC Reference: 4000-100N Intended Use: To evacuate air and/or fluid from the chest …

Atrium Medical Corporation

FDA Devices Moderate Feb 22, 2017

1.5mm System, Cranio-maxillofacial Bone Screws 1.5 x 4mm HT SD X-DR Screw, Bone Screw

Zimmer Biomet, Inc.

FDA Devices Moderate Feb 22, 2017

Discovery MR450 The systems are whole body magnetic resonance scanners designed to support high resolution, high signal-to-noise ratio, and short …

GE Healthcare, LLC

FDA Devices Moderate Feb 22, 2017

CentraLink¿ Data Management System Software Versions: v13x,v14x,v15x The CentraLink system software is a network solution provider and multi-syste…

Siemens Healthcare Diagnostics, Inc.

FDA Devices Moderate Feb 22, 2017

BrightView XCT

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Feb 22, 2017

Integra Cadence Total Ankle System

Integra LifeSciences Corp.

FDA Devices Moderate Feb 22, 2017

Stryker Restoris RIO Reamer Handle, Offset, Mako Rx only Product Usage: The handle is used to hold surgical components during acetabular reaming…

Mako Surgical Corporation

FDA Devices Moderate Feb 22, 2017

VIDAS 3 software v. 1.1.4

BioMerieux SA

CPSC Moderate Feb 22, 2017

Calphalon Recalls Cutlery Knives Due to Laceration Hazard

Calphalon Corp., of Atlanta, Ga.

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