PlainRecalls

2016 Recalls

6,806 recalls · Page 56 of 137

2016 Recall Year Insight

Federal agencies issued 6,806 product recalls indexed by PlainRecalls in calendar year 2016. That represents about 8.11% of the 83,949 total recalls we track from 1995 through the present, and averages roughly 18.6 recalls per day across the FDA, CPSC, NHTSA, and USDA FSIS 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 137 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 1 critical, 48 moderate, and 1 lower-severity recalls. The page references 13 distinct recalling firms operating in 2 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (47), FDA Drug (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 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, NHTSA, or USDA FSIS for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Drug Moderate Aug 24, 2016

Venlafaxine Hydrochloride Extended-Release Capsules, 150 mg, a) 30 capsules per bottle, NDC # 60429-123-30, b) 90 capsules per bottle, NDC # 60429-12…

Golden State Medical Supply Inc.

FDA Drug Moderate Aug 24, 2016

Venlafaxine HCL ER Capsule USP, 75mg, packaged in a) 30-count bottles (NDC 68382-035-06), b) 90-count bottles (NDC 68382-035-16), and c) 1000-count b…

Zydus Pharmaceuticals USA Inc

FDA Drug Moderate Aug 24, 2016

Venlafaxine Hydrochloride Extended-Release Capsules, 75 mg, 90 capsules per bottle, Rx Only, GSMS, NDC # 60429-122-90

Golden State Medical Supply Inc.

FDA Devices Moderate Aug 24, 2016

Certain Straight Healing Abutment 4.1mm(D) x 4.1mm(P) x 4mm(H) Item:ISHA44 Dental implants

Biomet 3i, LLC

FDA Devices Moderate Aug 24, 2016

Provide Protection Cap Dental implants

Biomet 3i, LLC

FDA Devices Moderate Aug 24, 2016

Certain Conical 25 degree Angled Abutment Dental implants

Biomet 3i, LLC

FDA Devices Low Aug 24, 2016

VITROS Immunodiagnostic Products TSH Reagent Pack, REF/Catalog Number/Product Code 191 2997, Unique Device Identifier No. 10758750000227, IVD --- Ort…

ORTHO-CLINICAL DIAGNOSTICS

FDA Devices Moderate Aug 24, 2016

AB Sciex API 3200MD" LC/MS/MS System. In-Vitro Diagnostic Instrument Part Number (REF): 5024501 3200MD series and 4500MD series are mass spectromet…

Ab Sciex

FDA Devices Moderate Aug 24, 2016

Certain Gingihue Post 4.1mm(D) x 5mm(P) x 4mm(H) Item: IAPP454G Dental implants

Biomet 3i, LLC

FDA Devices Moderate Aug 24, 2016

Perioscopy Sheath: Part number: 1008; The Perioscopy Sheath is a single-use sterile component used with the Perioscopy System, which is a med…

Danville Materials, Inc.

FDA Devices Moderate Aug 24, 2016

Certain Conical 17 degree Angled Abutment Dental implants

Biomet 3i, LLC

FDA Devices Moderate Aug 24, 2016

Certain Bellatek Encode Healing Abutment Dental implants

Biomet 3i, LLC

FDA Devices Moderate Aug 24, 2016

Certain Straight Pick-Up Coping 5.0mm(D) x 0mm(P) Item:IWIP50 Dental implants

Biomet 3i, LLC

FDA Devices Moderate Aug 24, 2016

Valleylab Laparoscopic Flexible Laparoscopic Argon Electrodes 3" Item Code: E25303 The Valleylab Laparoscopic Handset and Electrodes are indicated …

Medtronic

FDA Devices Moderate Aug 24, 2016

Conical EP Healing Cap Dental implants

Biomet 3i, LLC

FDA Devices Moderate Aug 24, 2016

Valleylab Laparoscopic Wire J-Hook Electrode 36CM Item Code: E277236 The Valleylab Laparoscopic Handset and Electrodes are indicated for use in la…

Medtronic

FDA Devices Moderate Aug 24, 2016

Certain Preformance 15 degrees Pre-Angled Post Dental implants

Biomet 3i, LLC

FDA Devices Moderate Aug 24, 2016

Certain Micromini Flat Implant Cover Screw Dental implants

Biomet 3i, LLC

FDA Devices Moderate Aug 24, 2016

Conical EP Twist Lock TM Coping Dental implants

Biomet 3i, LLC

FDA Devices Moderate Aug 24, 2016

Gingihue 15 degrees Pre-Angled Post 4mm(D) x 5mm(P) x 2mm(H) Item: PAP452G Dental implants

Biomet 3i, LLC

FDA Devices Moderate Aug 24, 2016

Valleylab Laparoscopic Flexible Laparoscopic Argon Blade Electrodes 28CM Item Code: E258028 The Valleylab Laparoscopic Handset and Electrodes are i…

Medtronic

FDA Devices Moderate Aug 24, 2016

DAL-RO Housing, Female Assembly Dental implants

Biomet 3i, LLC

FDA Devices Moderate Aug 24, 2016

GE Centricity PACS Workstation, versions 3.1.1.x through 3.2.1.x Picture Archiving and Communication System Used as a primary diagnostic and ana…

GE Healthcare It

FDA Devices Critical Aug 24, 2016

OraQuick Ebola Rapid Antigen Test, Product Code 3001-2807; Intended for the qualitative detection of antigens for Ebola viruses.

OraSure Technologies, Inc.

FDA Devices Moderate Aug 24, 2016

Certain EP Pick-Up Coping Dental implants

Biomet 3i, LLC

FDA Devices Moderate Aug 24, 2016

Valleylab Laparoscopic Wire J-Hook Electrode 45CM Item Code: E277345 The Valleylab Laparoscopic Handset and Electrodes are indicated for use in la…

Medtronic

FDA Devices Moderate Aug 24, 2016

DAL-RO Abutment Dental implants

Biomet 3i, LLC

FDA Devices Moderate Aug 24, 2016

TI Single Vector Distractor Proximal Foot/Left; Catalog ID 487.975 The Titanium Single Vector Distractor and Proximal Foot Plates are intended for…

Synthes (USA) Products LLC

FDA Devices Moderate Aug 24, 2016

Certain Pick-up Coping Dental implants

Biomet 3i, LLC

FDA Devices Moderate Aug 24, 2016

Valleylab Laparoscopic Flat L-Hook Electrode 28cm Item Code: E278428 The Valleylab Laparoscopic Handset and Electrodes are indicated for use in la…

Medtronic

FDA Devices Moderate Aug 24, 2016

Certain Gingihue 15 degree Angled Post Dental implants

Biomet 3i, LLC

FDA Devices Moderate Aug 24, 2016

Straumann Bone Level Implant, ¿ 4.1mm RC, SLA¿ 12mm, TiZr, NTP Article Number: 021.4512

Straumann Manufacturing, Inc.

FDA Devices Moderate Aug 24, 2016

Valleylab Laparoscopic Wire J-Hook Electrode 28CM Item Code: E278228 The Valleylab Laparoscopic Handset and Electrodes are indicated for use in la…

Medtronic

FDA Devices Moderate Aug 24, 2016

Certain Gingihue TM 15 degree Angled Post 3.4mm(D) x 3.8mm(P) x 2mm(H) Item: IMPAP32G Dental implants

Biomet 3i, LLC

FDA Devices Moderate Aug 24, 2016

Gold-Tite Square Uniscrew Item: UNISG Dental implants

Biomet 3i, LLC

FDA Devices Moderate Aug 24, 2016

Valleylab Laparoscopic Flat L-Hook Electrode Retractable Item Code: E2784R28ASP The Valleylab Laparoscopic Handset and Electrodes are indicated f…

Medtronic

FDA Devices Moderate Aug 24, 2016

LDA Screw SBL 3mm(D) Item: SCRSBL1 Dental implants

Biomet 3i, LLC

FDA Devices Moderate Aug 24, 2016

IOL Healing Cap Dental implants

Biomet 3i, LLC

FDA Devices Moderate Aug 24, 2016

Certain Standard Abutment Dental implants

Biomet 3i, LLC

FDA Devices Moderate Aug 24, 2016

IOL Distal Extension Dental implants

Biomet 3i, LLC

FDA Devices Moderate Aug 24, 2016

Certain EP Healing Abutment 4.1mm(D) x 5mm(P) x 2mm(H) Item: ITHA52 Dental implants

Biomet 3i, LLC

FDA Devices Moderate Aug 24, 2016

Synovis VASCU-GUARD Peripheral Vascular Patch in the following sizes and product codes: 1 cm x 6 cm, product code VG0106N, 0.8 cm x 8 cm, product…

Baxter Healthcare Corp.

FDA Devices Moderate Aug 24, 2016

1.5 mm HYDRO LeMaitre Valvulotome without LeMills, 98 cm. Sterile REF# 1009-00J Product Usage: The HYDRO LeMaitre Valvulotome is intended for th…

LeMaitre Vascular, Inc.

FDA Devices Moderate Aug 24, 2016

Certain Twist Lock TM Coping Dental implants

Biomet 3i, LLC

FDA Devices Moderate Aug 24, 2016

Temporary Hexed Cylinder Dental implants

Biomet 3i, LLC

FDA Devices Moderate Aug 24, 2016

Locator Replacement Males 4pk Dental implants

Biomet 3i, LLC

FDA Devices Moderate Aug 24, 2016

Gold Slotted Screw Dental implants

Biomet 3i, LLC

FDA Devices Moderate Aug 24, 2016

Valleylab Laparoscopic Wire L-Hook Electrode Retractable Item Code: E2783R36ASP The Valleylab Laparoscopic Handset and Electrodes are indicated fo…

Medtronic

FDA Devices Moderate Aug 24, 2016

1.5 mm HYDRO LeMaitre Valvulotome, 98 cm, Sterile REF # 1009-00 Product Usage: The HYDRO LeMaitre Valvulotome is intended for the treatment of …

LeMaitre Vascular, Inc.

FDA Devices Moderate Aug 24, 2016

Conical Abutment Gold Standard ZR TM Dental implants

Biomet 3i, LLC

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 + USDA FSIS — consumer product, vehicle, and meat/poultry recall feeds for 2016