PlainRecalls

2015 Recall Year Insight

Federal agencies issued 8,173 product recalls indexed by PlainRecalls in calendar year 2015. That represents about 7.83% of the 104,423 total recalls we track from 1995 through the present, and averages roughly 22.4 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 164 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 2015.

On this page of 50 records, severity classification shows 13 critical, 25 moderate, and 12 lower-severity recalls. The page references 28 distinct recalling firms operating in 5 distinct product categories, with 46 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (25), FDA Food (18), NHTSA (4), 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 2015 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 Devices Critical Dec 30, 2015

Etest¿ Piperacillin/tazobactam (4 ug/mL) PTc0.016-256-pack of 30 tests WW Etest¿ is a quantitative technique for determining the antimicrobial susceptibility of Gram-negative and Gram-positive aerobic bacteria.

Biomerieux

FDA Devices Low Dec 30, 2015

ProScreen CLIA Wvd 12 Panel Cup w/Adult., Item No. PSCupA-12M-W

Ameditech Inc

FDA Devices Moderate Dec 30, 2015

Reagent Management System (RMS) Dimension RxL Max HM STM Product Usage: The Reagent Management System (RMS) is a module for use with the Dimension¿ clinical chemistry system. The RMS doubles the available storage of refrigerated Flex¿ reagent cartridges on the Dimension¿ system from 44 to 88. The RMS loads, hydrates, and automatically removes Flex¿ reagent cartridges, allowing the Dimension¿ system to process samples without interruption.

Siemens Healthcare Diagnostics Inc.

FDA Devices Moderate Dec 30, 2015

Brilliance iCT SP Computed Tomography X-ray system

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Dec 30, 2015

Flexible Bone Awl; SJ607R; NON STERILE; B Braun Aesculap; Aesculap AG: These instruments are intended for use during the implantations of the A-Space SIBD and Arcadius XP L systems.

Aesculap, Inc.

FDA Devices Low Dec 30, 2015

RealityCHECK Tilt Cup 12 Panel + Adult, Item No. RC12TCA

Ameditech Inc

FDA Devices Moderate Dec 30, 2015

Zimmer UNIVERSAL Power System Loaner and Modular Electric/Battery Double Trigger Handpiece. Rx only Made in Switzerland

Zimmer, Inc.

FDA Devices Low Dec 30, 2015

iCup DX 11 Panel w/ Adulterant, Item No. I-DXA-1117-131

Ameditech Inc

FDA Devices Moderate Dec 30, 2015

Brilliance 64 Computed Tomography X-ray system

Philips Medical Systems (Cleveland) Inc

FDA Devices Low Dec 30, 2015

DrugSmart 9 Test Cup (BUP), Item No. 60960D

Ameditech Inc

FDA Devices Moderate Dec 30, 2015

VAPR¿ TRIPOLAR 90" Degree Suction Electrodes (Model/Catalog No: 225028)

DePuy Mitek, Inc., a Johnson & Johnson Co.

FDA Devices Low Dec 30, 2015

ProScreen CLIA Waived Cup 6 Drugs w/Adul, Item No. PSCupA-6MB-W

Ameditech Inc

FDA Devices Moderate Dec 30, 2015

Alaris EtCO2 Module, Model 8300. A capnograph that continuously monitors end tidal carbon dioxide (EtCO2), fractional inspired carbon dioxide (FiCO2), and respiratory rate (RR).

CareFusion 303, Inc.

FDA Devices Moderate Dec 30, 2015

MAGNETOM systems, magnetic resonance diagnostic devices (MRDD).

Siemens Medical Solutions USA, Inc

FDA Devices Low Dec 30, 2015

ImmuTest 12 Panel Dip Card, Item No. IMD-12MO3

Ameditech Inc

FDA Devices Low Dec 30, 2015

6 Panel Cup Body and Lid w/Adult (AU), Item No. TDDA-6MBAU-CUP

Ameditech Inc

FDA Devices Moderate Dec 30, 2015

IntellaTip MiFi XP Asymmetric (N4) Curve 7/110/2.5/8-10 OUS; Material Number: M004EPM4790N40; Catalog number: EPM4790N4; Cardiac: The IntellaTip MiFi XP Catheter is indicated for interruption of accessory atrioventricular conduction pathways associated with tachycardia, for treatment of AV nodal reentrant tachycardia, for treatment of atrial flutter tachycardia, and for creation of complete AV block in patients with a rapid ventricular response to an atrial arrhythmia typically chronic,

Boston Scientific Corp

FDA Devices Moderate Dec 30, 2015

Zimmer Oscillating Flat - TS ST Hub; 75mm x 19mm x 1.00/1.27mm; Synvasive Part No. 11-4770: Part No. 19075127YT1; Lot No. 45104 and 43054 Description: STRYK_76542K_19X75X1.27T General and Plastic Surgery: The oscillating surgical saw blade is intended for use with powered equipment to resect bone and/or cartilage in orthopedic procedures

Synvasive Technology Inc

FDA Devices Moderate Dec 30, 2015

MicroCutter Xchange 30 Blue Curved Tip Cartridge. Model Number: FG-025321; The MicroCutter XCHANGE 30 Blue Cartridge and MicroCutter XCHANGE 30 Blue Curved Tip Cartridge contain 316L stainless steel staples. The cartridges are used with the MicroCutter XCHANGE 30 Stapler, which is a single patient device. When the MicroCutter XCHANGE 30 Stapler is loaded with a MicroCutter XCHANGE 30 Cartridge, two double rows of 316L stainless steel staples are delivered while simultaneously transecting tissue

Cardica, Inc.

FDA Devices Low Dec 30, 2015

EDI BZO Uncut Sheet - Cup*, Item No. 160170

Ameditech Inc

FDA Devices Moderate Dec 30, 2015

Total Toe Instrument Kit, Labeled in part: "Instrument Set, 15mm Toe, Dorsal Flange Combi" Part Number: 9000-3002 The component in question is the hex driver (part number 2009-4001).

Arthrosurface, Inc.

FDA Devices Moderate Dec 30, 2015

Reagent Management System (RMS) Dimension EXL with LM Product Usage: The Reagent Management System (RMS) is a module for use with the Dimension¿ clinical chemistry system. The RMS doubles the available storage of refrigerated Flex¿ reagent cartridges on the Dimension¿ system from 44 to 88. The RMS loads, hydrates, and automatically removes Flex¿ reagent cartridges, allowing the Dimension¿ system to process samples without interruption.

Siemens Healthcare Diagnostics Inc.

FDA Devices Moderate Dec 30, 2015

Dressit-X, Radiopaque D-545, NDC 11004-545-40, Dental Use Only, Active Ingredients: Eugenol Oil

Rainbow Specialty & Health Products

FDA Devices Low Dec 30, 2015

ProScreen 6 Panel Cassette w/Adult (AU), Item No. PSPA-6MBAU

Ameditech Inc

FDA Devices Moderate Dec 30, 2015

Reagent Management System (RMS) Dimension RxL Max w/o HM Product Usage: The Reagent Management System (RMS) is a module for use with the Dimension¿ clinical chemistry system. The RMS doubles the available storage of refrigerated Flex¿ reagent cartridges on the Dimension¿ system from 44 to 88. The RMS loads, hydrates, and automatically removes Flex¿ reagent cartridges, allowing the Dimension¿ system to process samples without interruption.

Siemens Healthcare Diagnostics Inc.

CPSC No agency class Dec 30, 2015

KTM North America Recalls Competition Off-Road Motorcycles Due to Fire Hazard (Recall Alert)

KTM Motorrad AG, of Austria

CPSC No agency class Dec 30, 2015

Origin8 Recalls Folding Bicycles Due to Fall Hazard

NHTSA No agency class Dec 30, 2015

BMW,MINI 2016: STEERING:GEAR BOX (OTHER THAN RACK AND PINION)

BMW,MINI

CPSC No agency class Dec 29, 2015

Macy's Recalls Martha Stewart Stainless Steel Cookware; Injury Hazard with Frying Pans

NHTSA No agency class Dec 28, 2015

BMW 2015: ELECTRONIC STABILITY CONTROL (ESC)

BMW

NHTSA No agency class Dec 28, 2015

FERRARI 2016: FUEL SYSTEM, GASOLINE:DELIVERY:HOSES, LINES/PIPING, AND FITTINGS

FERRARI

NHTSA No agency class Dec 28, 2015

DODGE,JEEP 2011-2013: ELECTRICAL SYSTEM:WIRING

DODGE,JEEP

FDA Food Critical Dec 23, 2015

Single Curry Chicken Salad Wrap, Made Right Here, 7oz UPC 263126

Whole Foods Market Group Inc.

FDA Food Critical Dec 23, 2015

GORGEOUS MEMORY brand Daylily, NET WT: 10.6 oz. (300 g), UPC 6 932960 968806, Product of China --- MINHANG FOOD CO., LTD, 103 Eldridge St., New York City, NY 10002 --- Nutrition Facts: Serving Size: 1 tbsp (100g), Servings Per Container: 4

A & S Food Trading Inc.

FDA Food Critical Dec 23, 2015

Classic Deli Pasta Salad, Sold by weight UPC 260976

Whole Foods Market Group Inc.

FDA Food Moderate Dec 23, 2015

Conte's Gluten Free Wheat Free Cheese Ravioli With Marinara Sauce (French Labeling - Raviolis Au Fromage avec sauce Marinara) Net Wt. 340 g (12 Ounces) Conte's Pasta Co. Inc. 310 Wheat Road, Vineland, NJ 08360 800.211.6607 www.contespasta.com UPC 734153944458

Contes Pasta Company, Inc.

FDA Food Critical Dec 23, 2015

Classic Deli Pasta Salad, 14 oz UPC 0 36406 30264 6

Whole Foods Market Group Inc.

FDA Food Moderate Dec 23, 2015

Sprinkle King, Yellow Sanding Sugar,QYEL413.L32, UPC:Inner: 766818313403; Outer: 10766818313400, NET WT: 32 lb (14.51 kg).

Kerry Foods

FDA Food Critical Dec 23, 2015

219772 509998 MARKET DISTRICT APRICOT LOG

Giant Eagle, Inc.

FDA Food Critical Dec 23, 2015

Honey Mustard Pretzel Mix sold under the following brand and size: Girl Scouts, NET WT 7 oz. (198g).

A. L. Schutzman Company, Inc.

FDA Food Moderate Dec 23, 2015

Sprinkle King, Black Sanding Sugar, QBLK413.L32, UPC: Inner: 00766818310006 ; Outer: 10766818310003, NET WT: 32 lb (14.51 kg).

Kerry Foods

FDA Food Critical Dec 23, 2015

Heng Cheong Loong Co., Net Wt: 10 oz. (5g), Plastic Bag, Product of U.S.A, UPC 6-930481-211418

Tristar Food Wholesale Co Inc

FDA Food Moderate Dec 23, 2015

Kerry, Cinnamon Topical G4205, SS189, G4205.49, , UPC:Inner: 766818313403; Outer: 10766818313400, NET WT: 50 lb (22.68 kg).

Kerry Foods

FDA Food Low Dec 23, 2015

HEB Herb Seared Salmon, Broccoli, Rice SS

H E B

FDA Food Low Dec 23, 2015

HEB Herb Seared Salmon Herb SS and FS; Houston Culinary Center Herb Seared Salmon

H E B

FDA Food Low Dec 23, 2015

Combo Meal Tuna Salad SS

H E B

FDA Food Critical Dec 23, 2015

My Spice Sage Ground Flax Seed Meal under the following labels: 1) NET WT 4 oz. (113g) UPC# 00575004, 2) NET WT 16 oz. (454g) UPC# 00575016, 3) NET WT 50 pounds UPC# 00575111.

Zenobia Co.

FDA Food Moderate Dec 23, 2015

Sprinkle King, Green Sanding Sugar, Q35111.G32,, UPC: 10766818350023, NET WT: 320 lb (144.3 kg). Sprinkle King, Green Sanding Sugar, QGRN413.L32, UPC: 10766818311109/ 00766818311102, , NET WT: 32 lb (14.51kg). Sprinkle King, Green Sanding Sugar, QGRN433.440, UPC: 10766818321122 , NET WT: 40 lb (18.14 kg).

Kerry Foods

FDA Food Moderate Dec 23, 2015

Sprinkle King, Pink Sanding Sugar,QPIN413.L32, UPC:766818312000/ 10766818312007, NET WT: 32 lb (14.51 kg).

Kerry Foods

FDA Food Moderate Dec 23, 2015

Sprinkle King, White Coarse Sugar, 30621693.L32, UPC: Outer: 30763089281623 / Inner: 763089280601, ,NET WT: 32 lb (14.51 kg). DDA, WHITE CON AA DDA (Coarse White Sugar) , Q31320.L32, 01064873, 01064823 (net wt 8 lb), UPC: Outer: 29519151867 / Inner: 29519151850, NET WT 32 LB (14.51 kg). Sprinkle King, 40#MTO WHITE SUGAR GEMS (Coarse White Sugar), Q32322.440, UPS 1076618323225, NET WT 40 lb (18.14 kg). Sprinkle King, WHITE CON AA SUGAR (Coarse White Sugar), QWHI533.440 , UPS O

Kerry Foods

Nearby Recall Years

Browse recalls from adjacent calendar years to see how federal enforcement volume has shifted over time.

Compare 2015 with 2014 →

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 2015

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 2015 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.