Official U.S. recalls · explained plainly

Know if it’s recalled — and exactly what to do.

We pull official government recall records and translate each one into plain language: what happened, how serious it is, and the steps to take. No legalese.

Search by meaning, not just keywords — describe the product or the hazard and we’ll find matching recalls even when the official notice uses different words. Brand names and model numbers work too.

Latest recalls

76,825 found

⚠️ Use cautionMedical device
Baxter Healthcare Corporation recalls Hillrom VOLARA System P.CIRCUIT KIT (Single Patient Use Circuit), Model/Catalog Number REF M08085; Oscillation Lung
Hillrom recalls VOLARA System circuit kits with air and medication leaks that may cause oxygen drops. Affected units sold from 4/28/2025 onward; fix by ensuring nebulizer cup locks properly.
HillromMay 21, 2026
ℹ️ UnratedMedical device
Bard Access Systems, Inc. recalls 5605150 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr Triple-Lumen UDI-DI Code: 00801741086953 5605240
Bard Access Systems recalls specific Power-Trialysis dialysis catheters due to lidocaine ampoules manufactured under deficient practices. Affected units have UDI-DI codes and lot numbers listed. Consumers should check their catheter details and contact Bard for guidance.
Bard Access SystemsMay 21, 2026
✓ Lower riskMedical device
Boston Scientific Corporation recalls CRE Pro Wireguided 18-20mm 240cm
Boston Scientific recalls CRE Pro Wireguided 18-20mm 240cm catheters due to potential sterile pouch breaches in packaging. Affected units have specific lot numbers and expiration dates.
Boston ScientificMay 21, 2026
⛔ Stop using nowMedical device
Windstone Medical Packaging, Inc. recalls A M S, ALIGNED MEDICAL SOLUTIONS, Preop Kit-NS, Pack Number AMS18227, surgical convenience kit
Windstone Medical recalls Preop Kit-NS (Pack Number AMS18227) due to contaminated alcohol prep pads found during sterilization checks. Affected kits contain specific lot codes. Stop using immediately to avoid infection risks.
Windstone MedicalMay 21, 2026

Know if it’s recalled — and exactly what to do.

Latest recalls

Baxter Healthcare Corporation recalls Hillrom VOLARA System P.CIRCUIT KIT (Single Patient Use Circuit), Model/Catalog Number REF M08085; Oscillation Lung

Bard Access Systems, Inc. recalls 5605150 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr Triple-Lumen UDI-DI Code: 00801741086953 5605240

Boston Scientific Corporation recalls CRE Pro Wireguided 18-20mm 240cm

Windstone Medical Packaging, Inc. recalls A M S, ALIGNED MEDICAL SOLUTIONS, Preop Kit-NS, Pack Number AMS18227, surgical convenience kit

Windstone Medical Packaging, Inc. recalls A M S, ALIGNED MEDICAL SOLUTIONS, DSAEK Pack-RX, Pack Number AMS12394B, surgical convenience kit

Bard Access Systems, Inc. recalls 1174108 PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741154935 1295108 PowerPICC SOLO Catheter 5 Fr

Boston Scientific Corporation recalls CRE Wireguided 10-12mm 240cm

Laborie Medical Technologies Corp recalls Solar GI System (Water Perfusion); Product Name (Catalog Number): Solar GI LGI H2O, 12p, Trolley system (G3-6), Solar

Medline Industries, LP recalls Medline Convenience Kits: 1) MERCY MEDICAL CIRCUMCISION TRAY, Model Number: CIT6780; 2) CIRCUMCISION TRAY W/1.1CM

Medline Industries, LP recalls Medline Convenience Kits: 1) ARTERIAL LINE KIT, Model Number: ART890B; 2) ULTRASOUND GUIDED IV SECUREMENT SET, Model

Bard Access Systems, Inc. recalls 4380 ECONOMY SOFT TISSUE BIOPSY TRAY UDI-DI Code: 0110885403108563 4382A SOFT TISSUE BIOPSY TRAY UDI-DI Code:

Boston Scientific Corporation recalls CRE Pro Wireguided 8-10mm 240cm

Medline Industries, LP recalls Medline Convenience Kits: 1) OPHTHALMIC PACK W/LIDO, Model Number: DYNJ57922A

Boston Scientific Corporation recalls CRE Wireguided 18-20mm 240cm

Bard Access Systems, Inc. recalls CK000980A PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236150 P4254108 PowerMidline Catheter 4 Fr

Boston Scientific Corporation recalls CRE Wireguided 6-8mm 240cm

Bard Access Systems, Inc. recalls 7617408 Groshong NXT ClearVue Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741035258 The Groshong¿ NXT PICC provides

BD SWITZERLAND SARL recalls BD Connecta" BD Luer-Lok" 360 REF 394910 UDI-DI code: 00382903949106 BD Connecta" Stopcocks are used to administer

Baxter Healthcare Corporation recalls Hillrom VOLARA System P.CIRCUIT 5KIT AC, (Single Patient Use Circuit), Model/Catalog Number REF M08474; Oscillation

Windstone Medical Packaging, Inc. recalls A M S, ALIGNED MEDICAL SOLUTIONS, Thyroid FNA Pack-RX, Pack Number AMS17729, surgical convenience kit

Bard Access Systems, Inc. recalls OTP5000 THORA/PARA TRAY, 5FR, NON-VALVED UDI-DI Code: 0110885403284748 PIG1260T SAFE-T-CENTESIS TRAY 6FR X 16CM UDI-DI

Windstone Medical Packaging, Inc. recalls A M S, ALIGNED MEDICAL SOLUTIONS, Dr. Lewin Pack, Pack Number AMS7200D, surgical convenience kit

Medline Industries, LP recalls Medline Convenience Kits: 1) BLOCK TRAY, Model Number: DYNJRA1590

Boston Scientific Corporation recalls CRE Wireguided 15-18mm 240cm

Boston Scientific Corporation recalls CRE Wireguided 12-15mm 240cm

Medline Industries, LP recalls Medline Convenience Kits: 1) LUMBAR PUNCTURE CHOICE, Model Number: DYNDH1215

Bard Access Systems, Inc. recalls CK000662 PowerPICC SOLO HF Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741129674 Catheter stylets provide internal

Boston Scientific Corporation recalls CRE Wireguided 8-10mm 240cm

Medline Industries, LP recalls Medline Convenience Kits: 1) ARTERIAL ACCESS TRAY W/LIDOCAINE, Model Number: ART1145; 2) Universal Central/Art Line

Boston Scientific Corporation recalls CRE Pro Wireguided 6-8mm 240cm