PlainRecalls

2017 Recalls

6,356 recalls · Page 74 of 128

2017 Recall Year Insight

Federal agencies issued 6,356 product recalls indexed by PlainRecalls in calendar year 2017. That represents about 7.57% of the 83,949 total recalls we track from 1995 through the present, and averages roughly 17.4 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 128 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 7 critical, 36 moderate, and 7 lower-severity recalls. The page references 36 distinct recalling firms operating in 7 distinct product categories, with 47 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (21), FDA Food (9), FDA Drug (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 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 May 17, 2017

SJ SPICY DB Net Wt. 48 LBS INGREDIENTS: Spices including Mustard, Paprika***Wheat Flour***CONTAINS: SOY, WHEAT spicetec¿ FLAVORS & SEASONINGS 6 Sant…

Givaudan Flavours Corp

FDA Food Critical May 17, 2017

7-ELEVEN CAESAR SIDE SALAD 3 oz. packaged in clear plastic container

Del Monte Fresh Produce N.A., Inc. HQ

FDA Drug Moderate May 17, 2017

Clozapine Tablets USP, 25 mg, 100-count bottle (NDC 0093-4359-01), 500- count bottle (NDC 0093-4359-05), 100 Unit Dose Blisters per carton (NDC 0093-…

Teva Pharmaceuticals USA

FDA Drug Low May 17, 2017

Olanzapine Tablets, 7.5 mg, packaged in a) 30-count bottles (NDC 62756-553-83), b) 100-count bottles (NDC 62756-553-88), and c) 1000-count bottles (N…

Sun Pharmaceutical Industries, Inc.

FDA Drug Low May 17, 2017

Olanzapine Tablets, 2.5 mg, 1000-count bottles, Rx Only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Manufactured by: Su…

Sun Pharmaceutical Industries, Inc.

FDA Drug Moderate May 17, 2017

Buprenorphine HCI Injection, 0.3 mg/mL, 1 mL Single Dose Vial (NDC 42023-179-01), packaged in 1 mL x 5 Single Dose Vials per carton (NDC 42023-179-05…

PAR Sterile Products LLC

FDA Drug Low May 17, 2017

Mozobil (plerixafor injection) 24mg/1.2mL (20mg/mL), For Single Use Only, Rx Only, Manufactured by: Genzyme Corporation 500 Kendall Street, Cambridge…

Sanofi-Aventis U.S. LLC

FDA Drug Low May 17, 2017

PrednisoLONE Oral Solution USP, 15 mg/5mL, alcohol content: 5%(v/v) 240 mL bottle, Rx Only, Manufactured in Canada By: CONTRACT PHARMACEUTICALS LIMI…

Teva Pharmaceuticals USA

FDA Drug Low May 17, 2017

Olanzapine Tablets, 10 mg, packaged in a) 30-count bottles (NDC 62756-554-83), b) 100-count bottles (NDC 62756-554-88), and c) 1000-count bottles (ND…

Sun Pharmaceutical Industries, Inc.

FDA Drug Low May 17, 2017

Olanzapine Tablets, 20 mg, packaged in a) 30-count bottles (NDC 62756-556-83), b) 100-count bottles (NDC 62756-556-88), and c) 1000-count bottles (ND…

Sun Pharmaceutical Industries, Inc.

FDA Drug Low May 17, 2017

IC-Green (indocyanine green for injection, USP), 25 mg, packaged in a kit containing six vials of 25 mg lyophilized powder, Rx only, Manufactured by…

Akorn, Inc.

FDA Devices Moderate May 17, 2017

NDI P7 Position Sensor, Stereotaxic Instrument

Orthosoft, Inc. dba Zimmer CAS

FDA Devices Moderate May 17, 2017

Anthrex Bio-SwiveLock SP Vented, 5.5mm x 24.5 mm, Self-Punching

Arthrex, Inc.

FDA Devices Moderate May 17, 2017

RAPIDPoint¿ 500 Blood Gas Analyzer with v2.4 software for professional use in a point-of-care or laboratory environment. This system tests blood gase…

Siemens Healthcare Diagnostics Inc

FDA Devices Moderate May 17, 2017

Anthrex SpeedBridge Implant System with BioComposite SwiveLock SP Vented, 5.5 mm x 24 mm

Arthrex, Inc.

FDA Devices Moderate May 17, 2017

Healon GV, Part No. 10294701, 10294801, 10200014, 10201014, 10202014, 10203014

Abbott Medical Optics Inc. (AMO)

FDA Devices Moderate May 17, 2017

Stryker PROFESS Registration Kit. The Stryker PROFESS Registration Kit is a member of the Navigation portfolio and is used as an intraoperative guid…

Stryker Instruments Div. of Stryker Corporation

FDA Devices Moderate May 17, 2017

Healon Pro, Part No. 10270012

Abbott Medical Optics Inc. (AMO)

FDA Devices Moderate May 17, 2017

Mederi Stretta Catheter and Accessory Kit, Sterile For Use with the MEDERI MDRF1 GENERATOR ONLY. Used in the treatment of gastroesophageal reflux …

Mederi Therapeutics, Inc

FDA Devices Moderate May 17, 2017

Cobalt HV Bone Cement Cobalt MV Bone Cement Cobalt HV Bone Cement With Gentamicin

Zimmer Biomet, Inc.

FDA Devices Moderate May 17, 2017

Anthrex PEEK SwiveLock SP Vented, 5.5mm x 24.5 mm, Self-Punching

Arthrex, Inc.

FDA Devices Moderate May 17, 2017

Mentor Smooth Round SPECTRUM Post- Operatively Adjustable Saline Breast Implant, Product Code: 350-1490, UDI/GTIN: 00081317002048

Mentor Texas, LP.

FDA Devices Moderate May 17, 2017

Linear Straight Broach Handle (Rasp Handle) (Greatbatch Part # 510397; DJO Surgical Inc., # 803-03-159) and EZ Clean" Linear Broach Handle Greatbatc…

Greatbatch Medical

FDA Devices Moderate May 17, 2017

Medtronic PAK NEEDLE BEVELED AND TROCAR TIPS, REF 8670009, QTY 1 EA, STERILE R, Rx only

Medtronic Sofamor Danek USA Inc

FDA Devices Moderate May 17, 2017

MEDHOT MTI 2000 THERMAL IMAGING SYSTEM - TotalVision software with Elevated Body Temperature Screening module, for use as a medical diagnostic purpos…

Med-Hot Thermal Imaging, Inc.

FDA Devices Moderate May 17, 2017

Medi-Therm Hyper/Hypothermia System, MTA7900

Stryker Medical Division of Stryker Corporation

FDA Devices Moderate May 17, 2017

Healon 5 Pro, Part No. 10270015

Abbott Medical Optics Inc. (AMO)

FDA Devices Moderate May 17, 2017

Healon, Part No. 10290953, 10295210, 10200011, 10200012, 10201012, 10203012, 10213012, 10223012, 10290701, 10294751, 10295701

Abbott Medical Optics Inc. (AMO)

FDA Devices Moderate May 17, 2017

Regenerex Patella RGX 3 PEG SER A PATELLA 28MM RGX 3 PEG SER A PATELLA 31MM RGX 3 PEG SER A PATELLA 34MM RGX 3 PEG SER A PATELLA 37MM Product …

Zimmer Biomet, Inc.

FDA Devices Moderate May 17, 2017

Sample probes associated with: cobas 6000 Series System, cobas 8000 Modular Analyzer Series, cobas c 311 analyzer cobas c 501/502 cobas c 701/702…

Roche Diagnostics Corporation

FDA Devices Moderate May 17, 2017

Microfil Composite Instruments are packaged in an unsealed plastic sleeve, which is then placed in a cardboard box. Microfil Composite Instruments ar…

Almore International Inc

FDA Devices Moderate May 17, 2017

Healon Duet, Part No. 10290080, 10220010, 10220011 and 10220012

Abbott Medical Optics Inc. (AMO)

CPSC Moderate May 17, 2017

Cabrinha Recalls Kiteboard Control Systems Due to Injury and Fall Hazards

Cabrinha Kites, a subsidiary of Pryde Group Americas, of Doral, Fla.

CPSC Moderate May 17, 2017

Douglas Recalls Plush Toys Due to Choking Hazard

Douglas Company Inc., of Keene, N.H.

NHTSA Critical May 17, 2017

GMC,ISUZU 2008-2013: VEHICLE SPEED CONTROL:ACCELERATOR PEDAL

GMC,ISUZU

CPSC Moderate May 16, 2017

Bradshaw International Recalls Coffee Presses Due to Laceration Hazard

NHTSA Critical May 16, 2017

KENWORTH 2012-2018: SERVICE BRAKES, AIR

KENWORTH

CPSC Moderate May 15, 2017

VanMoof Recalls Bicycles Due to Fall and Impact Hazards

404 Park Partners LP, of New York

CPSC Moderate May 12, 2017

Honeywell International Recalls SWIFT® Wireless Gateway Sold with Fire Alarm Systems Due To Failure to Communicate in Fire

Honeywell International Inc., of Northford, Conn.

CPSC Moderate May 12, 2017

Little Passports Recalls Science Kits Due to Burn Hazard (Recall Alert)

Shenzhen Jiayuanwei Electronic Co. Ltd., of China

CPSC Moderate May 11, 2017

Carrier and Bryant Recall Heat Pumps Due to Fire Hazard

Carrier Corporation, of Jupiter, Fla.

CPSC Moderate May 11, 2017

Nature’s Truth Recalls Iron Supplement Bottles Due to Failure to Meet Child-Resistant Closure Requirement

Nature's Truth LLC, of Ronkonkoma, N.Y.

NHTSA Critical May 11, 2017

FREIGHTLINER 2017: POWER TRAIN:AXLE ASSEMBLY

FREIGHTLINER

FDA Food Critical May 10, 2017

ORIGINAL KB KILLER BROWNIE¿ 3x35 CT NET WT 36 LBS (16.33 kg) CONTAINS: Milk, Nuts: Pecans, Soy, Wheat UPC 10858061005031. Item #48-2016

Killer Brownie Distributing LLC

FDA Food Moderate May 10, 2017

Goya Octopus in Pickled Sauce, Pulpo a la Marinera, NET WT./PESO NETO 4 oz. (113g), PRODUCT OF SPAIN "WILD FISH", GOYA FOODS, INC., Secaucus N.J. 070…

Tradewind Foods de Puerto Rico Inc.

FDA Food Critical May 10, 2017

GERMAN CHOCOLATE KB KILLER BROWNIE¿ 3x35 CT NET WT 36 LBS (16.33 kg) CONTAINS: Milk, Nuts: Pecans, Soy, Wheat UPC 10858061005321. Item #483-2016

Killer Brownie Distributing LLC

FDA Food Critical May 10, 2017

Pre-cooked, chilled, Fresh Lump Crabmeat, 1 lb, packaged in plastic container with plastic lid. King Crab and Seafood De Venezuela, product of Venez…

Seafarers Inc.

FDA Food Moderate May 10, 2017

10.0 Grams Chili Spice Blend in packets

Arro Corporation

FDA Food Moderate May 10, 2017

Goya Octopus in Vegetable Oil, Pulpo en Aceite Vegetal, NET WT./PESO NETO 4 oz. (113g), PRODUCT OF SPAIN "WILD FISH", GOYA FOODS, INC., Secaucus N.J.…

Tradewind Foods de Puerto Rico Inc.

FDA Food Moderate May 10, 2017

Safeguard Flour product code 5122286 packaged in 50 lb bags

Ardent Mills Llc Usa

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