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 2 critical, 48 moderate, and 0 lower-severity recalls. The page references 13 distinct recalling firms operating in 3 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (30), FDA Food (16), FDA Drug (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 Food Moderate Aug 5, 2015

American Cheddar Flavor Slices: SOYA KAAS 12/8OZ AMERICAN CHEDDAR FLAVOR SLICES, 7801600480.

Dairy Farmers OF America Inc

FDA Food Moderate Aug 5, 2015

Imitation Pasteurized Process Cheese Food: . Sandwich MATE 12/10.67OZ Monterey JACK singles, IMIT WHT. 7103025182. Sandwich MATE 12/8OZ Monterey JACK singles, IMIT PP.99 WHT, 7103025185

Dairy Farmers OF America Inc

FDA Food Critical Aug 5, 2015

goodies by Nature RAW CASHEWS, NET WT. 9 oz (255g), held in clear plastic tubs, UPC code of 846034010055. Distributed By: Grand BK Corp. 47-08 Grand Ave. Maspeth, NY 11378. Product of India.

GRAND BK CORP.

FDA Food Moderate Aug 5, 2015

Pasteurized Prepared Cheese Product: BORDEN 12/12OZ WHITE AMER CHEESE PROD , 5300001636. CUMBERLAND 12/8OZ AMER CHEESE PROD WHITE, 4270401171

Dairy Farmers OF America Inc

FDA Food Moderate Aug 5, 2015

Reduced Fat Pasteurized Prepared Cheese Product: BORDEN 12/12OZ 2% SHARP CHEDDAR YELLOW, 5300000615.

Dairy Farmers OF America Inc

FDA Food Moderate Aug 5, 2015

Reduced Fat Pasteurized Prepared Cheese Product: BORDEN 12/12OZ 2PCT AMER WHT, 5300001614.

Dairy Farmers OF America Inc

FDA Food Moderate Aug 5, 2015

American Pasteurized Cheese Product: MARVELLA 12OZ 340G AMERICAN PASTEURIZED CHEESE, SINGLES, 5193319275.

Dairy Farmers OF America Inc

FDA Food Moderate Aug 5, 2015

Imitation Pasteurized Process Cheese Food: VALUE TIME 12/8OZ SANDWICH SLICES IMITATION PASTEURIZED PROCESS CHEESE FOOD, AMER IMIT YLW, 1122509140. VALUE TIME 12/10.67OZ SANDWICH SLICES IMITATION PASTEURIZED PROCESS CHEESE FOOD, AMER IMIT YLW, 1122558045. VALUE TIME 48/10.67OZ AMER IMIT YLW DS, 1122558045. CLEAR VALUE 48/10.67 OZ SANDWICH SLICES IMITATION PASTEURIZED PROC EES CHEESE FOOD AMER IMIT YLW, 3680012151. CLER VALUE 12/10.67OZ SANDWICH SLICES IMITATION PASTEURIZED PROCESS CHEESE

Dairy Farmers OF America Inc

FDA Food Moderate Aug 5, 2015

Pasteurized Prepared Cheese Product: SENSATIONS 12/8OZ SOUTHWEST PEPPER JACK WHT, 5300000990.

Dairy Farmers OF America Inc

FDA Food Moderate Aug 5, 2015

Reduced Fat Pasteurized Prepared Cheese Product: BORDEN 12/6.56OZ 2% LIGHT MOZZARELLA REDUCED FAT SLICES, 5300001605.

Dairy Farmers OF America Inc

FDA Food Critical Aug 5, 2015

Vegetable Chili, 8 oz plastic container, labeled with a green and white label with green and white lettering.

Brett Anthony Foods

FDA Food Moderate Aug 5, 2015

FLAVORED PASTEURIZED PREPARED CHEESE PRODUCT BORDEN SENSATIONS 12/8OZ APPLEWOOD BACON CHEDDAR 5300000980

Dairy Farmers OF America Inc

FDA Food Moderate Aug 5, 2015

Flavored Pasteurized Prepared Cheese Product: HYVEE 12/12OZ PEPPER JACK CHS PROD, 7545009334.

Dairy Farmers OF America Inc

FDA Food Moderate Aug 5, 2015

Atkins Chocolate Candies  5 ct. cartons - UPC code 637480075558

Atkins Indiana Distribution Center

FDA Food Moderate Aug 5, 2015

Atkins Chocolate Peanut Candies 5 ct. Case - UPC code 637480075770

Atkins Indiana Distribution Center

FDA Food Moderate Aug 5, 2015

Pasteurized Prepared Cheese Product: FOOD CLUB 12/12 OZ CHEEZY DOES IT, PASTEURIZED PREPARED CHEESE PRODUCT, 3680032338.

Dairy Farmers OF America Inc

FDA Drug Moderate Aug 5, 2015

Clonidine Hydrochloride Tablets, USP, 0.3 mg, 100 count HDPE bottles, Rx only, Mutual Pharmaceutical, Philadelphia, PA, NDC 53489-217-01

Mutual Pharmaceutical Company, Inc.

FDA Drug Moderate Aug 5, 2015

Clonidine Hydrochloride Tablets, USP, 0.1 mg, packaged in a) 100 count (NDC 53489-215-01) and b) 1000 count (NDC 53489-215-10) HDPE bottles, Rx only, Mutual Pharmaceutical, Philadelphia, PA

Mutual Pharmaceutical Company, Inc.

FDA Drug Moderate Aug 5, 2015

Clonidine Hydrochloride Tablets, USP, 0.2 mg, packaged in a) 100 count (NDC 53489-216-01) and b) 1000 count (NDC 53489-216-10) HDPE bottles, Rx only, Mutual Pharmaceutical, Philadelphia, PA.

Mutual Pharmaceutical Company, Inc.

FDA Drug Moderate Aug 5, 2015

COMBIVENT RESPIMAT (ipratropium bromide and albuterol) Inhalation Spray, 20 mcg/100 mcg per actuation*, 4 Grams, 120 Metered Doses per inhaler, Rx only, Distributed by Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT 06877 USA, Made in Germany, NDC 0597-0024-02.

Boehringer Ingelheim Roxane Inc

FDA Devices Moderate Aug 5, 2015

Medical Device Exchange PT WIRE 300; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number 38931-04; EXP (repackager), Boston Scientific (OEM) Wire, guide, catheter

EXP Pharmaceutical Services Corp

FDA Devices Moderate Aug 5, 2015

ANSPACH - 8MM x 12.5MM Fluted Barrel; REF M-8BA-G1 Cutting shaping bone including spine and cranium.

The Anspach Effort, Inc.

FDA Devices Moderate Aug 5, 2015

ANSPACH - Fluted Barrel; 8MM x 12.5MM REF L-8BA-G1 Cutting shaping bone including spine and cranium.

The Anspach Effort, Inc.

FDA Devices Moderate Aug 5, 2015

Paragon Laboratory Management

McKesson Technologies, Inc.

FDA Devices Moderate Aug 5, 2015

ANSPACH - 5MM Diamond Ball, 2MM Shaft Exposure; REF S-5D-2-G1 Cutting shaping bone including spine and cranium.

The Anspach Effort, Inc.

FDA Devices Moderate Aug 5, 2015

ANSPACH - Fluted Drum, Side Cut Only; 7MM x 14MM REF L-7DRC-G1 Cutting shaping bone including spine and cranium.

The Anspach Effort, Inc.

FDA Devices Moderate Aug 5, 2015

Medical Device Exchange 2.15MMX22MM Fluted Spiral Router for CRANI-A; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number A-CRN-S; EXP (repackager), Anspach (OEM) Bur, surgical, general & plastic surgery

EXP Pharmaceutical Services Corp

FDA Devices Moderate Aug 5, 2015

Hardy Diagnostics VRE Broth, 5ml container type: 16x100mm tube packaged: 20 tubes/box fill: 5ml Product Usage: BEA (Bile Esculin Azide) Broth with Vancomycin is for the surveillance of vancomycin resistant enterococci (VRE) not to be used for susceptibility reporting.

Hardy Diagnostics

FDA Devices Moderate Aug 5, 2015

Computed Tomography X-ray Systems Brilliance CT 64-channel with Essence technology. Intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Aug 5, 2015

Medical Device Exchange -Suction Coagulator; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number E2505-10FR; EXP (repackager), Valleylab (OEM) Electrosurgical, cutting & coagulation & accessories

EXP Pharmaceutical Services Corp

FDA Devices Moderate Aug 5, 2015

ANSPACH - 4MM Diamond Ball, Extends 27MM; REF S-4D-L-G1 all lot numbers Cutting shaping bone including spine and cranium.

The Anspach Effort, Inc.

FDA Devices Moderate Aug 5, 2015

Cortical Pin 2.0 mm,Sterile, FREEZE DRIED: Store at ambient temperature. Do Not freeze.

Musculoskeletal Transplant Foundation, Inc.

FDA Devices Moderate Aug 5, 2015

ANSPACH - Fluted Acorn, 7MM REF L-7AC-G1 Cutting shaping bone including spine and cranium.

The Anspach Effort, Inc.

FDA Devices Moderate Aug 5, 2015

Medical Device Exchange ETS FLEX 45 ENDOSCOPIC ARTICULATING LINEAR CUTTER, 45MM STAPLE; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number ATS45; EXP (repackager), Ethicon (OEM) Implantable Staple.

EXP Pharmaceutical Services Corp

FDA Devices Moderate Aug 5, 2015

OxiMax N-560 Pulse Oximeter. For continuous or spot check monitoring of functional arterial oxygen saturation (SpO2) and pulse rate.

Covidien LP (formerly Nellcor Puritan Bennett Inc.)

FDA Devices Moderate Aug 5, 2015

Medical Device Exchange SECURESTRAP 5mm Absorbable Strap Fixation Device; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number STRAP25; EXP (repackager), Ethicon (OEM) Strap, implantable.

EXP Pharmaceutical Services Corp

FDA Devices Moderate Aug 5, 2015

Medical Device Exchange Wire (sternotomy wire); Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number 046-072; 046-073; EXP (repackager), A & E Medical (OEM) Suture, nonabsorbable

EXP Pharmaceutical Services Corp

FDA Devices Moderate Aug 5, 2015

ANSPACH - Fluted Drum, Side Cut only, 6MM x 14MM REF L-6DRC-G1 Cutting shaping bone including spine and cranium.

The Anspach Effort, Inc.

FDA Devices Moderate Aug 5, 2015

ANSPACH - Extra Coarse Diamond Ball; 8MM REF L-8DX-G1 Cutting shaping bone including spine and cranium.

The Anspach Effort, Inc.

FDA Devices Moderate Aug 5, 2015

Computed Tomography X-ray systems Brilliance iCT, Philips Healthcare System. Intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Aug 5, 2015

Computed Tomography X-ray Systems Ingenuity CT scanners. Intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Aug 5, 2015

ANSPACH - 4MM x 11 MM Fluted Barrel, 14 Flutes; REF M-4BA-A-G1. Cutting shaping bone including spine and cranium.

The Anspach Effort, Inc.

FDA Devices Moderate Aug 5, 2015

Medical Device Exchange Round Diamond Bur Extra Coarse; 3.0mm; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number 5820-10-130; EXP (repackager), Stryker (OEM) Drills, burrs, trephines & accessories (simple, powered)

EXP Pharmaceutical Services Corp

FDA Devices Moderate Aug 5, 2015

Hardy Diagnostics BEA Agar with VGA container type: 15x100mm monoplate packaged: 10 places/sleeve Product Usage: BEA (Bile Esculin Azide) Agar with Vacomycin, Gentamicin, and Amphotericin B is for the selective isolation of vancomycin resistant enterococci (VRE).

Hardy Diagnostics

FDA Devices Moderate Aug 5, 2015

Hardy Diagnostics BHI with CIPRO, 1ug/ml container type: 16x100mm tube packaged: 20 tubes/box Product Usage: Brain Heart Infusion Broth with Ciprofloxacin, 1ug is for use as pre-enrichment broth for the cultivation of ciprofloxacin-resistant organisms from clinical samples.

Hardy Diagnostics

FDA Devices Moderate Aug 5, 2015

Medical Device Exchange Insufflation Needle; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number C2201; EXP (repackager), Medline (OEM) Insufflator, laparoscopic

EXP Pharmaceutical Services Corp

FDA Devices Moderate Aug 5, 2015

Medical Device Exchange - Endo Catch 10mm; Pouch, Tyvek/Mylar, Sterile, Single Use Only; OEM Catalog number 173050G; EXP (repackager), Auto Suture (OEM) Endoscope and Accessories

EXP Pharmaceutical Services Corp

FDA Devices Moderate Aug 5, 2015

Computed Tomography X-ray Systems Ingenuity Core. Intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Aug 5, 2015

Hardy Diagnostics MacConkey Agar with CiPRP, 1ug/ml Container type: 15x100mm monoplate packaged: 10 plates/sleeve Product Usage: MacConkey Agar with Ciprofloxacin is used as a screening medium for the selective isolation of Ciprofloxacin-resistant E. coli from clinical samples.

Hardy Diagnostics

FDA Devices Moderate Aug 5, 2015

ANSPACH - 2.3MM Fluted Matchstick, Extends 22MM; REF S-8N-L-G1 Cutting shaping bone including spine and cranium.

The Anspach Effort, Inc.

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.