PlainRecalls

2017 Recalls

7,480 recalls · Page 87 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 4 critical, 39 moderate, and 7 lower-severity recalls. The page references 30 distinct recalling firms operating in 5 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (29), FDA Food (10), 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 Black Pepper 42.75 lbs INGREDIENTS: Black Pepper, Spices including Mustard, Paprika***Wheat Flour***CONTAINS: SOY, WHEAT spicetec¿ FLAVORS & SEASO…

Givaudan Flavours Corp

FDA Food Moderate May 17, 2017

SJ MILD DB 36.33 LBS INGREDIENTS: Salt,***Wheat Flour***CONTAINS: SOY, WHEAT spicetec¿ FLAVORS & SEASONINGS 6 Santa Fe Way Cranbury, NJ 08512 (800) 3…

Givaudan Flavours Corp

FDA Food Moderate May 17, 2017

SJ TABASCO Net Wgt: 36.33 LBS INGREDIENTS: Spices including Mustard, Salt, Paprika***Wheat Flour***CONTAINS: SOY, WHEAT spicetec¿ FLAVORS & SEASONING…

Givaudan Flavours Corp

FDA Food Moderate May 17, 2017

Macaroni & Cheese microwaveable cups sold under the following brands: 1. Big Win Original Macaroni & Cheese Dinner, UPC 11822-58403. 2. Chees…

Treehouse Foods

FDA Food Critical May 17, 2017

Organic Cocoa-Dusted Chocolate Ginger, packaged and distributed in 5 lbs. bulk bag. Product was later offered to consumers in a self-serve bulk bin …

Hummingbird Wholesale

FDA Food Critical May 17, 2017

12 count Lays Kettle Cooked Multipack Sack 10.2 oz packaged in flexible plastic

Frito-Lay, Inc

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 Food Moderate May 17, 2017

Fresh Mozzarella; No brand name. Shipped in 30 lb. plastic bucket

Farmo Foods, Inc.

FDA Food Critical May 17, 2017

30 count Lays Kettle Cooked Multipack Tray 41.25 oz. packaged in flexible plastic

Frito-Lay, Inc

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)

FDA Devices Moderate May 17, 2017

PERI-LOC VOLAR DISTAL RADIUS - RIGHT 3H STD HEAD LOCKING PLATE, 62 MM LENGTH, SST PLATE, REF 71823114, QTY: (1) NON-STERILE, Rx only, Smith & nephew,…

Smith & Nephew, Inc.

FDA Devices Moderate May 17, 2017

Healon V, Part No. 10290045

Abbott Medical Optics Inc. (AMO)

FDA Devices Moderate May 17, 2017

Anthrex PEEK SwiveLock SP Vented, 4.75 mm x 24.5 mm, Self-Punching

Arthrex, Inc.

FDA Devices Moderate May 17, 2017

Bone Dowell Harvest Tubes

Zimmer Biomet, Inc.

FDA Devices Moderate May 17, 2017

CooperSurgical lnflatoball Latex Rubber Pessary sold as an individual unit and also part of the lnflatoball Pessary Kit. Product Usage: The lnfla…

CooperSurgical, Inc.

FDA Devices Moderate May 17, 2017

Anthrex Bio Composite SwiveLock SP Vented, 4.75 mm x 24.5 mm, Self-Punching

Arthrex, Inc.

FDA Devices Moderate May 17, 2017

Anthrex SpeedBridge Implant System with PEEK SwiveLock Self Punching

Arthrex, Inc.

FDA Devices Moderate May 17, 2017

Savaria SL-1000 Stairlift

Savaria Concord Lifts, Inc.

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.

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