Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

1176–1200 of 27375

HighFDA (Devices)·Z-1564-2026·2026-03-18
Medline surgical drapes may delaminate prematurely after recommended laundering
Medline is recalling five surgical drape products because the fabric may delaminate prematurely when the included laundering instructions are followed.
Product
Medline Surgical Drapes: MDTBTCS6070GN DBD-DRAPE,COVER,TABLE,RESIS/XALT GRN,60X MDTBTCS6090GN DBD-DRAPE,COVER,TABLE,RESIS/XALT GRN,60X MDTDXUNDBGN DBD-DRAPE,UNDERBUTTOCK,28 X 50.5,XALT GR MDTMAYOXGN DBD-DRAPE,COVER,MAYO STAND,RESISTAT/XALT MDTZ1003656GN DBD-POCKET SHEET,RESISTAT
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1516-2026·2026-03-18
Link Endo-Model plateau 15-2836/11 recalled over screw bushing fracture
Waldemar Link is recalling Endo-Model Replacement Plateau item 15-2836/11 because the bushing on a plateau screw could detach from the screw shaft due to a longitudinal fracture.
Product
Endo-Model Replacement Plateau; Item Number: 15-2836/11;
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1470-2026·2026-03-11
Abiomed Impella RP Flex recalled as Class I over sensor drift
Abiomed is recalling the Impella RP Flex with SmartAssist because the differential pressure sensor may malfunction, causing sensor values to drift. The FDA has classified this recall as Class I.
Product
Impella RP Flex with SmartAssist. Product Code: 1000323.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1469-2026·2026-03-11
Abiomed Impella RP with SmartAssist recalled as Class I
Abiomed is recalling the Impella RP with SmartAssist because the differential pressure sensor may malfunction, causing sensor values to drift. The FDA has classified this recall as Class I.
Product
Impella RP with SmartAssist. Product Code: 0046-0035.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1471-2026·2026-03-11
Abiomed Impella RP recalled as Class I over sensor malfunction risk
Abiomed is recalling the Impella RP, product code 0046-0011, because the differential pressure sensor may malfunction, causing sensor values to drift. The FDA has classified this recall as Class I.
Product
Impella RP. Product Code: 0046-0011.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1489-2026·2026-03-11
Olympus biopsy valve MAJ-1218 may shed rubber fragments during use
Olympus is recalling all lots of its Single Use Biopsy Valve, model MAJ-1218, because of the potential for rubber fragment detachment during use.
Product
Olympus Single Use Biopsy Valve. Model/Catalog Number: MAJ-1218. 20 units per box. The MAJ-1218 has been designed to be attached to the instrument channel port of compatible endoscopes to prevent leakage of body fluids.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1485-2026·2026-03-11
Aesculap MINOP trocar shafts may be longer than specified
Aesculap is recalling MINOP Trocar 150 mm with 6.0 mm working channel, model FF399R, because of the potential for the trocar shaft to be too long.
Product
Brand Name: AESCULAP Product Name: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Model/Catalog Number: FF399R Software Version: N/A Product Description: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1477-2026·2026-03-11
Olympus lithotripsy reusable probes recalled over generator transducer recognition failure
Olympus is recalling ShockPulse-SE Lithotripsy System reusable probes after further instances of the generator remaining in a blinking phase waiting to recognize the transducer.
Product
Brand Name: ShockPulse-SE Lithotripsy System SPL-SR Product Name: ShockPulse-SE Lithotripsy System - Reusable Probes Model/Catalog Number: SPL-SR Product Description: The ShockPulse Lithotripsy System is an electromechanical device capable of fragmenting calculi and aspirating
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1480-2026·2026-03-11
Implantable collamer lenses recalled after being labeled with wrong length
Staar Surgical is recalling seven EVO+ Visian Toric Implantable Collamer Lenses that were labeled as 12.1 mm but are 12.6 mm, creating the potential for excessive vault.
Product
EVO+ Visian Toric Implantable Collamer Lens (TICL), Model: VTICM5
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1491-2026·2026-03-11
Stago free protein S assay may underestimate normal range results
Diagnostica Stago is recalling four lots of the STA Liatest Free Protein S kit because of the potential for out-of-range results and underestimation of free protein S in normal patient plasmas.
Product
Brand Name: STA Liatest Free Protein S Product Name: STA Liatest Free Protein S Model/Catalog Number (REF): 00516 Product Description: The STA¿ - Liatest¿ Free Protein S kits are intended for use on STA-R¿ and STA Compact¿ for the quantitative antigenic assay of free protein S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1478-2026·2026-03-11
Olympus lithotripsy single use probes recalled over generator recognition failure
Olympus is recalling ShockPulse-SE Lithotripsy System single use probes after further instances of the generator remaining in a blinking phase waiting to recognize the transducer.
Product
Brand Name: ShockPulse-SE Lithotripsy System SPL-S Product Name: ShockPulse-SE Lithotripsy System - Single Use Probes Model/Catalog Number: SPL-S Product Description: The ShockPulse Lithotripsy System is an electromechanical device capable of fragmenting calculi and aspirating
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1475-2026·2026-03-11
GE radiology viewer may show patient information not matching displayed images
GE Healthcare is recalling Centricity Universal Viewer Zero Footprint Client because under certain workflows the patient information shown may not match the images displayed.
Product
GE Healthcare Centricity Universal Viewer Zero Footprint Client, Model Numbers: 2110344-039, 2110344-046, 2110344-047; System, Image Processing, Radiological
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1479-2026·2026-03-11
Olympus lithotripsy generator recalled over transducer recognition failure
Olympus is recalling the ShockPulse-SE Lithotripsy System Generator after further instances of the generator remaining in a blinking phase waiting to recognize the transducer.
Product
Brand Name: ShockPulse-SE Lithotripsy System Product Name: ShockPulse-SE Lithotripsy System - Generator Model/Catalog Number: SPL-G Product Description: The ShockPulse Lithotripsy System is an electromechanical device capable of fragmenting calculi and aspirating stone debris.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1494-2026·2026-03-11
Olympus lithotripsy systems recalled over mis-wired component causing electrical noise
Olympus is expanding a recall of ShockPulse-SE Lithotripsy Systems after finding additional generators with a mis-wired component that adds noise to the power supply output.
Product
Brand Name: Olympus ShockPulse-SE Lithotripsy System with Generator Product Name: ShockPulse-SE Lithotripsy System - Reuseable Probes Model/Catalog Number: SPL-SR, contains generator SPL-G Product Description: An assembly of devices that uses a combination of, or individually
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1488-2026·2026-03-11
Olympus single use biopsy valve may shed rubber fragments during use
Olympus is recalling all lots of its Single Use Biopsy Valve, model MAJ-210, because of the potential for rubber fragment detachment during use.
Product
Olympus Single use Biopsy Valve. Model/Catalog Number: MAJ-210. 20 units per box. The MAJ-210 has been designed to be attached to the instrument channel port of compatible endoscopes to prevent reflux of body fluids.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1481-2026·2026-03-11
B. Braun 21G 4.4 cm winged infusion needles may break
B. Braun Medical is recalling 21G x 4.4 cm Winged Infusion devices, model 7B3050, because the needle tip may be dull or blunt, difficult to advance, or may break.
Product
Brand Name: B. Braun Product Name: BBraun Medical 21G X4.4CM Winged INF Model/Catalog Number: 7B3050 Software Version: N/A Product Description: A device designed for subcutaneous implantation and intended to be used temporarily to expand an implanted tissue expander by percut
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1490-2026·2026-03-11
Esaote endocavity ultrasound probe recalled because liquid may leak in
Esaote is recalling five Endocavity ultrasonic probes, model E 3-12, because a potential weakness in the probe body may allow liquid to leak from the casing near the cable.
Product
Esaote Endocavity ultrasonic probe, Model E 3-12, REF 120000038
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1482-2026·2026-03-11
B. Braun 21GA winged infusion single packs may have blunt needles
B. Braun Medical is recalling 21GA Winged Infusion single packs, model 7A3842, because the needle tip may be dull or blunt, difficult to advance, or may break.
Product
Brand Name: B. Braun Product Name: 21GA WINGED INFUSION, SINGLE PK Model/Catalog Number: 7A3842 Software Version: N/A Product Description: A device designed for subcutaneous implantation and intended to be used temporarily to expand an implanted tissue expander by percutaneou
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1476-2026·2026-03-11
Roche cobas analyzer may repeat previous results for spline calibrated assays
Roche is recalling cobas pro sample supply units on software versions before 03-02 because a defect can make the analyzer repeat the last calculated result for all later measurements.
Product
cobas pro integrated solutions with cobas c 503 analytical units: cobas pro sample supply unit, material number 08464502001 cobas pro SSU, material number 09205632001 Affected Assays: (Product Name/ Catalog Number/ Application Code/ Application Short Name) 1. Cystati
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1483-2026·2026-03-11
B. Braun 21GA winged infusion sets may have blunt needle tips
B. Braun Medical is recalling 21GA Winged Infusion Sets, model 7M2802, because the needle tip may be dull or blunt, difficult to advance, or may break.
Product
Brand Name: B. Braun Product Name: 21GA WINGED INF SET Model/Catalog Number: 7M2802 Software Version: N/A Product Description: A device designed for subcutaneous implantation and intended to be used temporarily to expand an implanted tissue expander by percutaneous injection
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1484-2026·2026-03-11
Siemens urine albumin assay may report falsely depressed patient results
Siemens Healthcare Diagnostics is recalling all lots of the Atellica CH Urine Albumin assay because falsely depressed patient results may occur above the measuring interval.
Product
Atellica CH Urine Albumin (UAlb). Material Number: 11537225
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1429-2026·2026-03-04
Hitachi Proton Beam Therapy System Recall Over Positioning Software Issue
Hitachi is recalling one Proton Beam Therapy System due to a software anomaly in the patient positioning system that may cause positional discrepancy during treatment.
Product
Brand Name: Hitachi Proton Beam Therapy System Ref: PROBEAT-FR
Category
Medical Device
Distribution
2 states
SevereFDA (Devices)·Z-1453-2026·2026-03-04
Olympus Inner Sheath 21 Fr. Model A2660T Medical Device Recall
Olympus is recalling all lots of its Inner Sheath 21 Fr. Model A2660T used in urological procedures due to reports of the ceramic tip breaking during use.
Product
Olympus Inner Sheath 21 Fr. Model No. A2660T. for endoscopic diagnosis and treatment in urological applications.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1474-2026·2026-03-04
Remel Campy CVA Medium Lot Recalled Over Low Pathogen Recovery
Remel, Inc is recalling 97 units of Campy CVA Medium 100/PK, lot R01272, due to customer complaints reporting low to no recovery of Campylobacter Jejuni ATCC 33291. The product was distributed nationwide in AZ, CO, IL, NJ, OH, TN, and WA.
Product
Campy CVA Medium 100/PK, R01272
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1459-2026·2026-03-04
Knee and Humeral Socket Implants Recalled for Incorrect Labeling
Encore Medical, LP is recalling 14 EMPOWR 3D KNEE implants because they contain incorrect labeling. The recall affects US nationwide distribution.
Product
Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 7L 16MM, VE Model/Catalog Number: 341-16-707
Category
Medical Device
Distribution
Distributed nationwide

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1176–1200 of 27375