PlainRecalls

2026 Recalls

2,438 recalls · Page 36 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 5 critical, 39 moderate, and 6 lower-severity recalls. The page references 15 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 (39), FDA Drug (11), 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 Drug Moderate Feb 18, 2026

ESTRADIOL,15 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-3015-32.

F.H. INVESTMENTS, Inc. (dba Asteria Health)

FDA Drug Moderate Feb 18, 2026

Testosterone, 50.0 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-1050-32.

F.H. INVESTMENTS, Inc. (dba Asteria Health)

FDA Drug Moderate Feb 18, 2026

Cetrorelix Acetate for Injection (Kit), 0.25 mg per vial, Single-Dose Kit, Rx Only, Mfd. for: Meitheal Pharmaceuticals, Chicago, IL NDC 71288-558-90.

Meitheal Pharmaceuticals, Inc

FDA Drug Moderate Feb 18, 2026

Testosterone, 37.5 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-1037-32.

F.H. INVESTMENTS, Inc. (dba Asteria Health)

FDA Drug Moderate Feb 18, 2026

ESTRADIOL, 18 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 3521, NDC: 79559-3018-32.

F.H. INVESTMENTS, Inc. (dba Asteria Health)

FDA Drug Moderate Feb 18, 2026

Testosterone 87.5mg, Triamcinolone Acetonide17.5 mcg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-6087-32.

F.H. INVESTMENTS, Inc. (dba Asteria Health)

FDA Drug Moderate Feb 18, 2026

Pro Numb Tattoo Numbing Spray, For Sensitive Skin, 4% Lidocaine, [1FL OZ/28.4 ML or 4 oz/120 mL] per bottle, Distributed by: Pro Numb Tattoo numbing …

Pro Numb Tattoo Numbing Spray LLC

FDA Drug Moderate Feb 18, 2026

ESTRADIOL, 22 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-3022-32.

F.H. INVESTMENTS, Inc. (dba Asteria Health)

FDA Drug Moderate Feb 18, 2026

Testosterone 100mg Anastrozole 4mg , 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-4104-32

F.H. INVESTMENTS, Inc. (dba Asteria Health)

FDA Drug Moderate Feb 18, 2026

Testosterone 75mg, Anastrozole 4mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-4079-32.

F.H. INVESTMENTS, Inc. (dba Asteria Health)

FDA Drug Moderate Feb 18, 2026

ESTRADIOL, 6 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-3006-32.

F.H. INVESTMENTS, Inc. (dba Asteria Health)

FDA Devices Moderate Feb 18, 2026

Brand Name: Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system Software Version: 11,3, 11.4 Product Description: Leksell Ga…

Elekta, Inc.

FDA Devices Low Feb 18, 2026

Surepulse VS Cap Large REF: SP-162-A1 component of VS Newborn Heart Rate Monitor

SUREPULSE MEDICAL LTD

FDA Devices Moderate Feb 18, 2026

Medline medical convenience kits packaged as: 1) POWERGLIDE DRESSING CHANGE KIT, Kit SKU DYNDH1576; 2) CENTRAL LINE TRAY W/ CHLRP SWB, Kit SKU R…

Medline Industries, LP

FDA Devices Low Feb 18, 2026

Surepulse VS Cap Medium REF: SP-161-A1 component of VS Newborn Heart Rate Monitor

SUREPULSE MEDICAL LTD

FDA Devices Moderate Feb 18, 2026

Brilliance iCT; Product Code (REF): 728306;

Philips North America Llc

FDA Devices Moderate Feb 18, 2026

Spectral CT; Product Code (REF): 728333;

Philips North America Llc

FDA Devices Critical Feb 18, 2026

Reprocessed Abbott Inquiry Steerable Diagnostic Catheters: Abbott Inquiry Steerable Diagnostic Catheter 10 Elec. 2-5-2mm 81105RH 81172RH; A…

Medline Industries, LP

FDA Devices Moderate Feb 18, 2026

Azurion 7 M12 System Model Numbers: (1)722078, (2)722223, (3)722233; Software Version Number - All versions: R1.X, R2.X, R3.X

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 18, 2026

Medline 14 Fr Suction Catheter Kits SKU DYND40972 - respiratory convenience kit

Medline Industries, LP

FDA Devices Moderate Feb 18, 2026

Azurion 7 M20 System Model Numbers: (1)722079, (2)722224, (3)722234, (4)722282(OUS only); Software Version Number - All versions: R1.X, R2.X, R3.X

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Critical Feb 18, 2026

Medline ReNewal Reprocessed Webster CS Catheters: Webster CS Catheter 10 Electrodes 2-8-2mm Spacing w/AutoID w/ EZ Steer BD710DF282CRH; Webster …

Medline Industries, LP

FDA Devices Moderate Feb 18, 2026

Azurion 7 B12 System Model Numbers:(1) 722067, (2) 722225, (3) 722235; Software Version Number - All versions: R1.X, R2.X, R3.X

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Critical Feb 18, 2026

Reprocessed Siemens ACUSON AcuNav Diagnostic Ultrasound Catheters: ACUSON AcuNav Ultrasound Catheter, Use on GE Systems 10135910RH; 10043342RH …

Medline Industries, LP

FDA Devices Moderate Feb 18, 2026

Laerdal Compact Suction Unit 4 RTCA version (LCSU 4 RTCA) 1) LCSU 4, 800 ml, RTCA; Catalog Number: 880052; 2) LCSU 4, 300 ml, RTCA; Catalog Num…

Laerdal Medical Corporation

FDA Devices Moderate Feb 18, 2026

da Vinci 5 Surgeon Console Viewer Display, ASSY, DV5 CONSOLE, IS5000, Part Number: 380730-45

Intuitive Surgical, Inc.

FDA Devices Moderate Feb 18, 2026

Medline medical convenience kits packaged as: PEDIATRIC CATH SECUREMENT DRSG, Kit SKU DYNDC3108

Medline Industries, LP

FDA Devices Moderate Feb 18, 2026

Azurion 5 M12 System Model Numbers: (1)722227, (2)722231; Software Version Number - All versions: R1.X, R2.X, R3.X

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 18, 2026

Halyard TRANSPORT BAG KIT. Kit Code: LIFE0080-01.

AVID Medical, Inc.

FDA Devices Moderate Feb 18, 2026

Azurion 3 M15 System Model Numbers: (1) 722064, (2) 722222, (3) 722230, (4)722280(OUS only); Software Version Number - All versions: R1.X, R2.X, R3…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 18, 2026

IQon Spectral CT; Product Code (REF): 728332;

Philips North America Llc

FDA Devices Moderate Feb 18, 2026

ATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm REF 267-01-000-10-N UDI-DI code: 00190376541471; GMDN 12844 The ATEC Navig…

Alphatec Spine, Inc.

FDA Devices Low Feb 18, 2026

WB Impression Post Closed Tray incl. guide screw, L 13mm, TAN/POM

Straumann USA LLC

FDA Devices Critical Feb 18, 2026

Reprocessed St. Jude Supreme and Response Diagnostic Electrophysiology Catheters: St. Jude Medical Supreme Diagnostic Electrophysiology Catheter 4…

Medline Industries, LP

FDA Devices Moderate Feb 18, 2026

Azurion 3 M12 System Model Numbers: (1) 722063, (2) 722221, (3) 722229; Software Version Number - All versions: R1.X, R2.X, R3.X

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 18, 2026

Medline medical convenience kits packaged as: SUTURE REMOVAL TRAY, Kit SKU DYNDR1277A

Medline Industries, LP

FDA Devices Low Feb 18, 2026

Surepulse VS Cap Small REF: SP-160-A1 component of VS Newborn Heart Rate Monitor

SUREPULSE MEDICAL LTD

FDA Devices Moderate Feb 18, 2026

Medline medical convenience kits packaged as: ANESTHESIA ARTLINE PACK, Kit SKU DYNJ47387B

Medline Industries, LP

FDA Devices Moderate Feb 18, 2026

Azurion 7 B20 System Model Numbers: (1)722068, (2)722226, (3)722236; Software Version Number - All versions: R1.X, R2.X, R3.X

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Moderate Feb 18, 2026

Barco MNA with the HexaVue IP Integration System, Model/Catalog Number: MNA-6x0-H

Steris Corporation

FDA Devices Moderate Feb 18, 2026

Medline medical convenience kits packaged as: ) LVAD DRESSING CHANGE TRAY, Kit SKU DM320C; 2) PORT AND IO ACCESS DRESSING KI, Kit SKU DT15780A; …

Medline Industries, LP

FDA Devices Moderate Feb 18, 2026

Brand Name: Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system Software Version: 11.1 Product Description: Leksell GammaPla…

Elekta, Inc.

FDA Devices Moderate Feb 18, 2026

Azurion 5 M20 System Model Numbers: (1)722228, (2)722232, (3)722281(OUS only); Software Version Number - All versions: R1.X, R2.X, R3.X

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

FDA Devices Low Feb 18, 2026

Surepulse VS Cap Extra Small REF: SP-159-A1 component of VS Newborn Heart Rate Monitor

SUREPULSE MEDICAL LTD

FDA Devices Moderate Feb 18, 2026

Intubation Tray (Adult) containing Suction Catheter Kits SKU DYNJAA245B

Medline Industries, LP

FDA Devices Low Feb 18, 2026

Surepulse VS Cap Extra Large REF: SP-163-A1 component of VS Newborn Heart Rate Monitor

SUREPULSE MEDICAL LTD

FDA Devices Moderate Feb 18, 2026

ATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm REF 266-01-000-10-N UDI-DI code: 00190376476179; GMDN 12844 The ATEC Navig…

Alphatec Spine, Inc.

FDA Devices Moderate Feb 18, 2026

Medline medical convenience kits packaged as: STERILE RESUTURE PACK, Kit SKU DYNDL1980A

Medline Industries, LP

FDA Devices Moderate Feb 18, 2026

Brevera Breast Biopsy System Disposable 9 Gauge Needle. Biopsy Instrument.

Hologic, Inc

FDA Devices Critical Feb 18, 2026

Reprocessed Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheters: Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheter Use on G…

Medline Industries, LP

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.