2015 Recalls
8,173 federal recalls indexed for 2015 · Page 1 of 164
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 5 critical, 18 moderate, and 27 lower-severity recalls. The page references 22 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 Devices (39), FDA Food (5), 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.
PETERBILT 2015: TIRES
PETERBILT
Du Monde Gourmet Recalls Jafflz Sandwich Products Due To Possible Cooling/Process Deviation
Jafflz LLC
Basma 3 Chris Court Dayton, New Jersey 08810 Tel.:7323559600 Fax: 7323559644 16 oz package This golden raisin product is labeled in a foreign language.
UNITED TRADING CENTER INC
Winn Dixie Old Fashioned Potato Salad, Net Wt. 16oz (1 LB) 454g.
Reser's Fine Foods Inc.
TRC Golden Medium Raisins Packed by: The Raisin Company (PTY) LTD FActory AT: Noagspaal, Marchand, South Africa PO BOx 77, Marchand 8873 Produce of South Africa
UNITED TRADING CENTER INC
Salted Smoked Split Herring in bulk wooden boxes, Net Wt. 18 lbs., Product of Canada --- No label provided for bulk product.
P East Trading Corporation
Fat Bastard Gourmet Chick Dip Honey Roasted Hickory Smoke Sassy Barbecue, Net Wt. 12 Fl. Oz. (375 ml), UPC 8 91929 12702 8. The responsible firm name on the label is The Family Jewels, Montreal, MO 65591.
The Family Jewels LLC
HPMC Visoelastic Topical, 8,000 cps, Reference 5200, 1.5 mL in 3-mL Syringe, OASIS Medical Inc, 514 South Vermont Avenue Glendora, CA 91741
Oasis Medical, Inc.
HPMC Visoelastic, 8,000 cps, Reference 51082, LT5108 (Private Label), 2.0 mL in 3-mL Syringe, OASIS Medical Inc, 514 South Vermont Avenue Glendora, CA 91741
Oasis Medical, Inc.
Cetirizine HCl 10 mg Tablet, 14 count blister packs, sold over the counter under the following brands, GoodSense brand distributed by Perrigo, Allegan, MI; Equaline brand distributed by; Supervalu Inc, Eden Prairie, MN (NDC 41163-458-66); Good Neighbor Pharmacy brand, distributed by AmerisourceBergen, Chesterbrook, PA (NDC 24385-998-74); HEB brand, San Antonio, TX (NDC 37808-458-66); Rexall brand Packaged for Dolgencorp LLC, Goodlettsville, TN (NDC 55910-699-66 UPC: 370030659432), HyVee brand, d
Perrigo Company PLC
HPMC Visoelastic, 20,000 cps, Reference 5122, 515 (Private Label), 600102-001 (Private Label), 600103-001 (Private Label), 2.0 mL in 3-mL Syringe, OASIS Medical Inc, 514 South Vermont Avenue Glendora, CA 91741
Oasis Medical, Inc.
DrugSmart Cup 10, Item No. 61093D-3C, 61085D, 61015D
Ameditech Inc
Mobile X-ray system MobileDaRt Evolution/FDR Go Software The device is a mobile X-ray system and allows a technician to take a general digital radiography of patients in the hospital or medical facility who cannot move and outpatients in emergency.
Shimadzu Medical Systems
11 Panel Card (OPI 300) w/Adult, Item No. 71125AA
Ameditech Inc
ImmuTest Cup 7-panel w/ Adulteration, Item No. IMCA-7P
Ameditech Inc
ProScreen CLIA Waived Cup with 6 Drugs, Item No. PSCup-6BO-W
Ameditech Inc
Enterococcus Screen Agar QUAD Plate
Becton Dickinson & Co.
Immutest 12 Panel Cup w/Adulteration, Item No. IMCA-11OP
Ameditech Inc
Immutest 10 Pnl Drug Screen Cup w/ Adult, Item No. IMCA-10M5
Ameditech Inc
Hook Blade, Angled. Part number 7058A. Sterile disposable blade for use with Endoscopic Tarsal Tunnel Decompression (ETTD) System.
Instratek, Incorporated
ProScreen Cup CLIA with 6 Panel Drug, Item No. PSCup-6MB-W
Ameditech Inc
10-Panel Pipette Drug Screen, Item No. PSP-10M
Ameditech Inc
Ingenuity CT Computed Tomography X-ray system
Philips Medical Systems (Cleveland) Inc
Etest¿ PIP/TAZO/CON-4 PTC 256 - Foam of 100 tests US. Etest¿ is a quantitative technique for determining the antimicrobial susceptibility of Gram-negative and Gram-positive aerobic bacteria.
Biomerieux
iCup DX 6 Panel w/Adulterant, Item No. I-DXA-167-013
Ameditech Inc
Aegis Torque Handle CATALOG NO. : 2871-10-800. A spinal surgical instrument used on the AEGIS Anterior Lumbar Plate System.
DePuy Spine, Inc.
BZO Strip Dip Card (300ng/ml)*, Item No. 100170
Ameditech Inc
Brilliance iCT Computed Tomography X-ray system
Philips Medical Systems (Cleveland) Inc
1 Step 12 Panel Cup, Item No. NBCA-12M-W
Ameditech Inc
ProScreen 10 Drug Panel Cassette Test, Item No. PSP-10PPX
Ameditech Inc
DrugSmart 11 Test Cup, Item No. 61127D
Ameditech Inc
iCup DX 12 Panel w/ Adulterant, Item No. I-DXA-1127-023
Ameditech Inc
ProScreen 12 Drug Cup w/Adulteration, Item No. PSCupA-12TBU
Ameditech Inc
Flexible Screw Driver SJ706R; 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.
Immutest 5 Pnl Drug Cup w/ Adult -waived, Item No. IMCA-5AB-W
Ameditech Inc
Syngo Imaging XS is a Picture Archiving and Communication System (PACS)
Siemens Medical Solutions USA, Inc
ProScreen 9 Panel Cup w/Adulterants, Item No. PSCUPA-9BO300
Ameditech Inc
Vancomycin Screen Agar
Becton Dickinson & Co.
DrugSmart Dip (MET/OPI2)+AMP+BZO+COC+THC, Item No. 30600D
Ameditech Inc
ProScProScreen 10 Panel Cup with Adulterants, Item No. PSCupA-10AM
Ameditech Inc
Zimmer UNIVERSAL Power System Loaner and Modular Electric/Battery Single Trigger Handpiece. Rx only Made in Switzerland
Zimmer, Inc.
ProScreen 10 Panel Dip Card, Item No. PSD-10MOX, PSD-10MOB, PSD-10MMO300
Ameditech Inc
Flexible Drill; SJ723R; 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.
Label reading in part as: "NexGen System, Complete Knee Solution; Reference Number 5980-37-01; Tibial Component, Precoat, Stemmed Size 3; Lot Number:62460264. Indicated for patients with severe knee pain and disability and is intended for mating with a UHMWPE articular surface and Zimaloy Cobalt-Chromium-Molybdenum alloy femoral component to perform knee arthroplasty.
Zimmer Manufacturing B.V.
ProScreen 10 Panel Cup, Item No. PSCup-10M
Ameditech Inc
IntellaTip MiFi XP Asymmetric (N4) Curve 7/110/2.5/8-8 Material Number: M004PM4500N40; Catalog number: PM4500N4; 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, drug re
Boston Scientific Corp
Dressol-X, Radiopaque D-502, NDC 11004-502-40, Dental Use Only, Active Ingredients: A.S.A. (Acetylsalicylic Acid) + Eugenol
Rainbow Specialty & Health Products
iCup DX 8 Panel w/Adulterant, Item No. I-DXA-187-016
Ameditech Inc
Black Mamba Suture Passer
Biomet, Inc.
ProScreen 12 Panel Cup w/Adult., Item No. PSCupA-12M
Ameditech Inc
Nearby Recall Years
Browse recalls from adjacent calendar years to see how federal enforcement volume has shifted over time.
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.