PlainRecalls

2026 Recalls

Compiled from official public sources by the editorial team.

2,438 recalls · Page 28 of 49

2026 Recall Year Insight

Federal agencies issued 2,438 product recalls indexed by PlainRecalls in calendar year 2026. That represents about 2.40% of the 101,704 total recalls we track from 1995 through the present, and averages roughly 6.7 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 49 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 2026.

On this page of 50 records, severity classification shows 2 critical, 40 moderate, and 8 lower-severity recalls. The page references 17 distinct recalling firms operating in 1 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (50), 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 2026 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 Devices Low Mar 18, 2026

Penner Pacific Bathing Spa, Model Numbers 360030-1C, 360030-1CE, 360030-1CTS, 360030-XCE, 360030-XC, 360030-1CT, 360030-1C, 360030-XC, 360030-XCT, 36…

Penner Patient Care, Inc.

FDA Devices Moderate Mar 18, 2026

GEM Premier 5000 PAK; Part No. 00055360011.

Instrumentation Laboratory

FDA Devices Moderate Mar 18, 2026

DxC 700 AU, REF: B86444, B86446

Beckman Coulter Mishima K.K.

FDA Devices Moderate Mar 18, 2026

PHYSIO CONTROL INFANT/CHILD Reduced Energy Defibrillator Electrodes Catalog Numbers: 11101-000016 UDI-DI code: 00721902629013 Catalog Number: 11…

Physio-Control, Inc.

FDA Devices Moderate Mar 18, 2026

Brand Name: APTUS Product Name: 2.5 TriLock Screw 16mm, HD7, 1/Pkg Model/Catalog Number: A-5750.16/1 Software Version: Not applicable. Product De…

Medartis AG

FDA Devices Moderate Mar 18, 2026

GEM Premier 5000 PAK; Part No. 00055407508.

Instrumentation Laboratory

FDA Devices Moderate Mar 18, 2026

GEM Premier 5000; Part No. 00055445008.

Instrumentation Laboratory

FDA Devices Moderate Mar 18, 2026

GEM Premier 5000 PAK; Part No. 00055407510.

Instrumentation Laboratory

FDA Devices Moderate Mar 18, 2026

GEM Premier 5000 PAK; Part No. 00055360008.

Instrumentation Laboratory

FDA Devices Critical Mar 18, 2026

Owner's Booklets and Instructions for Use that are used with the following blood glucose measuring devices. Description/Item: Walgreens TRUE METRIX…

Trividia Health, Inc.

FDA Devices Moderate Mar 18, 2026

GEM Premier 5000; Part No. 00055445004.

Instrumentation Laboratory

FDA Devices Moderate Mar 18, 2026

GEM Premier 5000; Part No. 00055415010.

Instrumentation Laboratory

FDA Devices Moderate Mar 18, 2026

Artelon FLEXBAND TWIST .12 Ref: TW012 3.85x17mm HEX Anchor (Qty 2) 5.0x17mm HEX Anchor (Qty 1) 0.5x12cm FLEXBAND (Qty 1)

International Life Sciences

FDA Devices Moderate Mar 18, 2026

MEDLINE UNNA-Z STRETCH ZINC PASTE BANDAGE, REF NONUNNAS40 KOB article #40307010

KOB GmbH

FDA Devices Moderate Mar 18, 2026

Artelon FlexBand Plus Ref: 41054 & 41057

International Life Sciences

FDA Devices Moderate Mar 18, 2026

GEM Premier 5000; Part No. 00055430004.

Instrumentation Laboratory

FDA Devices Low Mar 18, 2026

Penner Pacific Bathing Spa, Model Numbers 760010-1, 770010-1

Penner Patient Care, Inc.

FDA Devices Moderate Mar 18, 2026

HealthCast "Vital Sync" Remote Patient Monitoring System which consists of: Product Number: VSLBASE03P / VITALSYNCSW03 Model / UDI-DI codes: Vita…

Covidien LLC

FDA Devices Low Mar 18, 2026

Penner Pacific Bathing Spa, Model Numbers 360010-2WT, 360010-1, 370000-1W, 360010-1WT, 362010-1, 370000-1WL, 360010-1L, 360010-1W, 360010-XWTL, 37000…

Penner Patient Care, Inc.

FDA Devices Low Mar 18, 2026

Penner Pacific Bathing Spa, Model Numbers 361910-1A, 361910-1A, 361910-XA, 361910-2I, 361910-1A, 361910-1, 361910-XI, 361910-1I, 361910-2A, 36191-1A…

Penner Patient Care, Inc.

FDA Devices Moderate Mar 18, 2026

Endo-Model Replacement Plateau; Item Number: 15-0027/15;

Waldemar Link GmbH & Co. KG (Mfg Site)

FDA Devices Low Mar 18, 2026

Penner Pacific Bathing Spa, Model Numbers 860010-1L

Penner Patient Care, Inc.

FDA Devices Moderate Mar 18, 2026

GEM Premier 5000; Part No: 00055415011.

Instrumentation Laboratory

FDA Devices Low Mar 18, 2026

Penner Pacific Bathing Spa, Model Numbers 560010-2L, 560010-XL, 560010-1L, 560010-XL

Penner Patient Care, Inc.

FDA Devices Moderate Mar 18, 2026

Clearest Strep-A Cassette Test. Test to determine the presence of group A streptococci (Strep A) in throat swab samples.

Altruan GmbH

FDA Devices Moderate Mar 18, 2026

10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. 850 bulk non-sterile units per case.

Becton Dickinson & Company

FDA Devices Critical Mar 18, 2026

Owner's Booklets and Instructions for Use that are used with the following blood glucose measuring devices. Description/Item: Walgreens TRUE METRI…

Trividia Health, Inc.

FDA Devices Moderate Mar 18, 2026

Brand Name: Equinoxe Product Name: Equinoxe Core Instrument Kit Model/Catalog Number: KIT-311X

Exactech, Inc.

FDA Devices Low Mar 18, 2026

Penner Pacific Bathing Spa, Model Numbers 350010-1, 350000-2, 350010-X

Penner Patient Care, Inc.

FDA Devices Moderate Mar 18, 2026

IBA Proton Therapy System - PROTEUS 235

Ion Beam Applications S.A.

FDA Devices Moderate Mar 18, 2026

Endo-Model Replacement Plateau; Item Number: 15-2835/12;

Waldemar Link GmbH & Co. KG (Mfg Site)

FDA Devices Moderate Mar 18, 2026

GEM Premier 5000; Part No. 00055430011.

Instrumentation Laboratory

FDA Devices Moderate Mar 18, 2026

Medline Medcrest Surgical Gowns: MDTGXC4J5XL DBQ-GOWN,SURG,XALT,L4, CRTCL CVR, GRN, 5 MDTGXC4JL DBD-GOWN,SURG,XALT,L4,CRTCL CVR,GREEN,L MDTGXC4J…

Medline Industries, LP

FDA Devices Moderate Mar 18, 2026

Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/07;

Waldemar Link GmbH & Co. KG (Mfg Site)

FDA Devices Moderate Mar 18, 2026

Endo-Model Replacement Plateau; Item Number: 15-2836/11;

Waldemar Link GmbH & Co. KG (Mfg Site)

FDA Devices Moderate Mar 18, 2026

Medline Surgical Drapes: MDTBTCS6070GN DBD-DRAPE,COVER,TABLE,RESIS/XALT GRN,60X MDTBTCS6090GN DBD-DRAPE,COVER,TABLE,RESIS/XALT GRN,60X MDTDXUNDBGN D…

Medline Industries, LP

FDA Devices Moderate Mar 18, 2026

CLARITY II Laser System; Model No. 1110200210.

Lutronic Corporation

FDA Devices Moderate Mar 18, 2026

GEM Premier 5000 PAK; Part No. 00055360010.

Instrumentation Laboratory

FDA Devices Moderate Mar 18, 2026

GEM Premier 5000 PAK; Part No. 00055415004.

Instrumentation Laboratory

FDA Devices Moderate Mar 18, 2026

GEM Premier 5000; Part No. 00055445010 & 00055445011.

Instrumentation Laboratory

FDA Devices Moderate Mar 18, 2026

Endo-Model SL Connection Component incl. PE-Plateau; Item Number: 16-2840/02;

Waldemar Link GmbH & Co. KG (Mfg Site)

FDA Devices Moderate Mar 18, 2026

Brand Name: APTUS Product Name: 2.8 TriLock Screw 16mm, HD7, 1/Pkg Model/Catalog Number: A-5850.16/1 Software Version: Not applicable. Product De…

Medartis AG

FDA Devices Moderate Mar 18, 2026

Brand Name: Bisaf Strep A Self-Test. Test for detection of group A streptococcal antigens in throat swabs.

Altruan GmbH

FDA Devices Low Mar 18, 2026

Penner Pacific Bathing Spa, Model Numbers 390010-1, 390010-X, 390010-2

Penner Patient Care, Inc.

FDA Devices Moderate Mar 18, 2026

Endo-Model Replacement Plateau; Item Number: 15-8521/09;

Waldemar Link GmbH & Co. KG (Mfg Site)

FDA Devices Moderate Mar 18, 2026

Wondfo Streptococcal A At-Home Self-Test. At-home test for group A beta-hemolytic streptococcal infection.

Altruan GmbH

FDA Devices Moderate Mar 18, 2026

EndoVive Safety PEG Kit; Outer Box Material Number (UPN): M00509001; Inner Box Material Number (UPN): M00509000;

Boston Scientific Corporation

FDA Devices Moderate Mar 18, 2026

GEM Premier 5000 PAK; Part No. 00055407504.

Instrumentation Laboratory

FDA Devices Moderate Mar 18, 2026

Endo-Model Replacement Plateau; Item Number: 15-8521/11;

Waldemar Link GmbH & Co. KG (Mfg Site)

FDA Devices Moderate Mar 18, 2026

Endo-Model Replacement Plateau; Item Number: 15-0027/12;

Waldemar Link GmbH & Co. KG (Mfg Site)

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: CPSC + NHTSA - consumer product and vehicle recall feeds for 2026

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Figures cover calendar year 2026 across the FDA, CPSC 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 July 2026.