PlainRecalls

2017 Recall Year Insight

Federal agencies issued 7,681 product recalls indexed by PlainRecalls in calendar year 2017. That represents about 7.36% of the 104,423 total recalls we track from 1995 through the present, and averages roughly 21.0 recalls per day across the FDA, CPSC, USDA FSIS, 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 154 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 10 critical, 34 moderate, and 6 lower-severity recalls. The page references 25 distinct recalling firms operating in 4 distinct product categories, with 49 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Food (24), FDA Devices (19), FDA Drug (7), 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, USDA FSIS, or NHTSA for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Food Critical Jan 18, 2017

FH Parmesan. Product Code: T206486-50. 50 lb bags

All American Seasonings, Inc.

FDA Food Moderate Jan 18, 2017

Koi Palace Mini Moon Cake: Mini Fresh Five Nuts with Smoked Ham Unit Size 1/2 lb. and 1/4 lb. in circular box (1 piece) and rectangular boxes (4, 6 or 8 pieces).

Magic Gourmet Trading Inc

FDA Food Moderate Jan 18, 2017

Charles Chocolates Toffee Chocolate Macadamia; NET WT. 6.2 oz .(180 grams) UPC: 8 59033 00440 6 Charles Chocolates, San Francisco, CA

Chocolate Holdings Inc. DBA Charles Chocolates

FDA Food Moderate Jan 18, 2017

Garden season no salt, 5 lb plastic gallon, product number 63516; Garden season no salt, 1.25 lb plastic jar, product number 63514

PIAZZA PRODUCE, INC.

FDA Food Critical Jan 18, 2017

Sabra Hummus SF Rosemary/Sea Salt, 10OZ; UPC 040822342988, SKU 301566

Sabra Dipping Company, LLC

FDA Food Critical Jan 18, 2017

Xtra Sharp Cheese Sauce. Product Code: T4015. 37.5 lb bags

All American Seasonings, Inc.

FDA Food Low Jan 18, 2017

Blackened seasoning, 5.5 lb plastic gallon, product number 61703; Blackened seasoning, 1.5 lb plastic jar, product number 61684; Blackened seasoning, 10 lb plastic pail, product number 61722

PIAZZA PRODUCE, INC.

FDA Food Critical Jan 18, 2017

Sabra Hummus Taco, 10OZ; UPC 040822343671; SKU 301640

Sabra Dipping Company, LLC

FDA Food Critical Jan 18, 2017

Sabra Hummus 3 Pepper Chili, 10OZ; UPC 040822344043; SKU301705

Sabra Dipping Company, LLC

FDA Food Critical Jan 18, 2017

Sabra Hummus Olive, 10OZ; UPC 040822011341; SKU 300117

Sabra Dipping Company, LLC

FDA Food Moderate Jan 18, 2017

Koi Palace Mini Moon Cake: Single Box - Mini Walnut, Red Bean Paste Unit Size 1/2 lb. and 1/4 lb. in circular box (1 piece) and rectangular boxes (4, 6 or 8 pieces).

Magic Gourmet Trading Inc

FDA Food Moderate Jan 18, 2017

NEW HOPE MILLS Crepe MIX, NET WT. 1 LB. 4 OZ, UPC 074703601529 --- 181 York Street, Auburn, New York 13021 ---Product is packaged in a brown paper bag

New Hope Mills Mfg., Inc.

FDA Food Low Jan 18, 2017

Taco seasoning, 5.5 lb plastic gallon, product number 68667; Taco seasoning, 1.5 lb plastic jar, product number 68665

PIAZZA PRODUCE, INC.

FDA Food Critical Jan 18, 2017

Chipotle Ranch ASI. Product Code: T3883. 33 lb bags

All American Seasonings, Inc.

FDA Food Moderate Jan 18, 2017

Fajita seasoning, 9 lb plastic gallon, product number 63545; Fajita seasoning, 2.5 lb plastic jar, product number 63543

PIAZZA PRODUCE, INC.

FDA Food Critical Jan 18, 2017

Sabra Hummus Spinach/Art, 10 OZ, 17 OZ, 32OZ UPC SKU ITEM 040822027700 300266 Sabra Hummus Spinach/Art 32OZ 040822027588 300298 Sabra Hummus Spinach/Art 17OZ 040822027540 300164 Sabra Hummus Spinach/Art 10OZ

Sabra Dipping Company, LLC

FDA Food Critical Jan 18, 2017

Sabra Hummus Pine Nut, 7 OZ, 10 OZ, 17 OZ, 32 OZ UPC SKU ITEM 040822011747 300132 Sabra Hummus Pine Nut 10OZ 040822127530 300134 Sabra Hummus Pine Nut 7OZ 040822990011 300136 Sabra Hummus Pine Nut 17OZ 040822012157 300139 Sabra Hummus Pine Nut 32OZ 040822990011 300501 Sabra Hummus Pine Nut 17OZ

Sabra Dipping Company, LLC

FDA Food Moderate Jan 18, 2017

Lemon Pepper, 5 lb plastic gallon, product number 65085; Lemon Pepper, 1.25 lb plastic jar, product number 65066; Lemon Pepper, 12 lb plastic pail, product number 65104

PIAZZA PRODUCE, INC.

FDA Food Moderate Jan 18, 2017

Cardboard sleeve: Cheese Club express mac Macaroni & Cheese Dinner, Four 2.05 OZ Bowls; Net Wt. 8.2 OZ.; Distributed by: Aldi, Inc., Batavia, IL 60510

Fourth Street Barbeque, Inc.

FDA Food Moderate Jan 18, 2017

Quebec Steak seasoning, 1.5 lb plastic jar, product number 67783; Quebec Steak seasoning, 6 lb plastic gallon, product number 67802; Quebec Steak seasoning, 10 lb plastic pail, product number 67821

PIAZZA PRODUCE, INC.

FDA Food Critical Jan 18, 2017

French Onion Seasoning ASI. Product Code: T3933. 33 lb bags

All American Seasonings, Inc.

FDA Food Low Jan 18, 2017

Onion salt, 9 lb plastic gallon, product number 65845; Onion salt, 2.5 lb plastic jar, product number 65826; Onion salt, 20 lb plastic pail, product number 65864

PIAZZA PRODUCE, INC.

FDA Food Moderate Jan 18, 2017

Italian Herb seasoning, 6 lb plastic pail, product number 64688; Italian Herb seasoning, 1.5 lb plastic gallon, product number 64667; Italian Herb seasoning, 6 oz plastic jar, product number 64648; Italian Herb seasoning, 3 lb plastic pail, product number 64686

PIAZZA PRODUCE, INC.

FDA Food Moderate Jan 18, 2017

Koi Palace Mini Moon Cake: Luxury Single Mooncake - Mini White Lotus Seed Paste w/ Egg Yolk Unit Size 1/2 lb. and 1/4 lb. in circular box (1 piece) and rectangular boxes (4, 6 or 8 pieces).

Magic Gourmet Trading Inc

FDA Drug Moderate Jan 18, 2017

Daytrana (methylphenidate transdermal system) Transdermal Patch, 20 mg over 9 hours (2.2 mg/hr), packaged in 30-count patches per box, Rx only, Manufactured by Noven Therapeutics, LLC, Miami, FL 33186; By Noven Pharmaceuticals, Inc., Miami, FL 33186, NDC 68968-5554-3.

Noven Pharmaceuticals, Inc.

FDA Drug Low Jan 18, 2017

HCG-Vitamin B12 5000 IU-8 mg in 10 mL vial, Rx only, For Sub-Q & IM Injection, Pharm D Solutions, Loop West Houston, TX --- NDA 69699-1723-20

Pharm D Solutions, LLC

FDA Drug Moderate Jan 18, 2017

10% Premasol sulfite-free (Amino Acid) Injection, 2000 mL bulk package, Rx only, Baxter Healthcare Corporation, Clintec Nutrition Division, Deerfield, IL 60015 USA, NDC 0338-1130-06

Baxter Healthcare Corporation

FDA Drug Moderate Jan 18, 2017

Daytrana (methylphenidate transdermal system) Transdermal Patch, 30 mg over 9 hours (3.3 mg/hr), packaged in 30-count patches per box, Rx only, Manufactured by Noven Therapeutics, LLC, Miami, FL 33186; By Noven Pharmaceuticals, Inc., Miami, FL 33186, NDC 68968-5555-3.

Noven Pharmaceuticals, Inc.

FDA Drug Low Jan 18, 2017

Testosterone Cypionate 200 mg/mL in Sesame Oil, 4 mL and 5 mL vials, Rx only, For IM injection, Pharm D Solutions, Loop West Houston, TX --- NDA 69699-1709-04

Pharm D Solutions, LLC

FDA Drug Low Jan 18, 2017

Cytotec (misoprostol) Tablets, 200 mcg, 100 Tablets blister pack (10X10), For in-institution use only, Rx only, Distributed by G.D. Searle, Division of Pfizer, Inc., NY, NY --- NDC 0025-1461-34

Pfizer Inc.

FDA Drug Moderate Jan 18, 2017

Daytrana (methylphenidate transdermal system) Transdermal Patch, 10 mg over 9 hours (1.1mg/hr), packaged in- 30 count per box, Rx only, Manufactured by Noven Therapeutics, LLC, Miami, FL 33186; By Noven Pharmaceuticals, Inc, Miami, FL 33186, NDC 68968-5552-3

Noven Pharmaceuticals, Inc.

FDA Devices Moderate Jan 18, 2017

Bio mCT-S(40) 3R->4R Upgrade, Material Number 10250743 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic information. The CT component produces cross-sectional images of the body by computer reconstruction of X-Ray transmission data from either the same axial plane taken at different angles or spiral planes taken at di

Siemens Medical Solutions USA Inc.

FDA Devices Moderate Jan 18, 2017

symmetry surgical ULTRA(R) Steam container, REF numbers: C131310, C13134, C13135, C13136, C13139, C13854, C13855, C13856, C181310, C18134, C18135, C18136, C18138, C22854, C22855, C22856, C22858, C24134, C24135, C24136 Product Usage: sterilization container

Symmetry Surgical, Inc.

FDA Devices Moderate Jan 18, 2017

Biograph mCT-X w/TrueV Upgrade, Material Number 10250745 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic information. The CT component produces cross-sectional images of the body by computer reconstruction of X-Ray transmission data from either the same axial plane taken at different angles or spiral planes taken at

Siemens Medical Solutions USA Inc.

FDA Devices Moderate Jan 18, 2017

i.v. Station and i.v. Station ONCO Automated Drug Compounding System, Pharmacy Compounding System Device Listing Number E454448

HEALTH ROBOTICS S.R.L.

FDA Devices Moderate Jan 18, 2017

GoDirect Screw-Retaining Top Part Numbers: 4500-61

Implant Direct Sybron Manufacturing, LLC

FDA Devices Moderate Jan 18, 2017

OPT Croutons is a synthetic bone substitute designed for the repair of bony defects and is made of pure beta-tricalcium phosphate. The tricalcium phosphate is a soluble calcium phosphate salt.

Acumed LLC

FDA Devices Moderate Jan 18, 2017

AxIEM Touch N Go Pointer Probe. Model Number: 9735318. Placed in a 30mil PETG tray sealed with a Tyvek lid and then placed in a shelf carton.

Medtronic Navigation, Inc.

FDA Devices Moderate Jan 18, 2017

DxH 600 Coulter Cellular Analysis System, Catalog No. B23858

Beckman Coulter Inc.

FDA Devices Moderate Jan 18, 2017

Biograph mCT S(40)-4R, Material Number 10248671 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic information. The CT component produces cross-sectional images of the body by computer reconstruction of X-Ray transmission data from either the same axial plane taken at different angles or spiral planes taken at different

Siemens Medical Solutions USA Inc.

FDA Devices Moderate Jan 18, 2017

SafeStep¿ Huber Needle Set with Y-Injection Site. Product Code: LH-0029YN. Packaged as single units in thermoformed trays. There are 25 SafeStep¿ trays per case and 100 per carton. Product Usage: Intended for the administration of fluids and drugs, or blood sampling through surgically implanted vascular ports.

Bard Access Systems

FDA Devices Moderate Jan 18, 2017

SCREW 02.7-12MM LOCKING, REF W27 ST112: a) DRP, b) NEO, In2Bones, 28 chemin du petit bois, 69130 Ecully - France The NEOVIEW¿ Plating System is intended for fixation of intra-articular and extraarticular fractures of the distal radius and reconstruction of the distal radius

In2Bones, SAS

FDA Devices Moderate Jan 18, 2017

Brilliance iCT Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analysts and display equipment, patient and equipment supports, components, and accessories

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Jan 18, 2017

Monaco RTP System Product Usage: Used to make treatment plans for patients with prescriptions for external beam radiation therapy.

Elekta, Inc.

FDA Devices Moderate Jan 18, 2017

NEO SCREW 02.7-14MM LOCKING, REF W27 ST114, In2Bones, 28 chemin du petit bois, 69130 Ecully - France The NEOVIEW¿ Plating System is intended for fixation of intra-articular and extraarticular fractures of the distal radius and reconstruction of the distal radius

In2Bones, SAS

FDA Devices Moderate Jan 18, 2017

StatLock¿ PICC Plus Crescent Foam. Product Code: VPPCSP & VPPCSPCE. Packaged as a single unit with a skin protectant pad and foam strips in a Tyvek pouch. Depending on configuration, there are either 25 or 50 pouches per carton and 10 cartons per case. Other configurations may contain additional components such as a foam pad with a pigtail clip. Product Usage: The StatLock¿ PICC Plus and StatLock¿ CV Plus catheter stabilization devices are suture-free stabilization devices for peripherally i

Bard Access Systems

FDA Devices Moderate Jan 18, 2017

133" 60 Drop 24 Hour Primary Set w/2 Bravo24¿, 2 Gang 1o2¿ Manifold, Rotating Luer, 1 Ext, Item No. B59006 Product Usage: The intravascular administration set is a single use, sterile, non-pyrogenic device which provides access for the administration of fluids from a container to a patient s vascular system through the administration set s needle or catheter (which is inserted into a vein). Each set will be manufactured to a unique specifications using dimensions, components and configuratio

ICU Medical, Inc.

FDA Devices Moderate Jan 18, 2017

SURESTEP Tray, BARDEX I.C. COMPLETE CARE, Urine Meter, Temperature STATLOCK Stabilization Device

C.R. Bard, Inc.

FDA Devices Moderate Jan 18, 2017

Biograph mCT S(64)-4R, Material Number 10248672 The Siemens Biograph mCT and Biograph mCT Flow systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic information. The CT component produces cross-sectional images of the body by computer reconstruction of X-Ray transmission data from either the same axial plane taken at different angles or spiral planes taken at different

Siemens Medical Solutions USA Inc.

FDA Devices Moderate Jan 18, 2017

OEC 9800. MDL Numbers: D222250, D141598 The OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical and interventional procedures. Clinical application may include cholangiography, endoscopy, urologic, orthopedic, neurologic, vascular, cardiac, critical care and emergency room procedures.

GE OEC Medical Systems, Inc

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: USDA FSIS Recalls - calendar-year meat, poultry, and processed egg product recall filings
  • Source: CPSC + NHTSA - consumer product and vehicle recall feeds for 2017

Every figure on PlainRecalls is rendered directly from official FDA, CPSC, USDA FSIS and NHTSA recall records; no number is typed in by an editor. Figures cover calendar year 2017 across the FDA, CPSC, USDA FSIS and NHTSA federal recall feeds. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of September 2026.