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Consumer Product Recalls
127,244 recalls from the U.S. Consumer Product Safety Commission, newest first.
April 29, 2026Medical DevicesFDA
LSL Healthcare Inc. recalls LSL Healthcare, Infant Central Line Dressing Change Kit, Model/Catalog Number: 2925H
Hazard: Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
April 29, 2026Medical DevicesFDA
LSL Healthcare Inc. recalls LSL Healthcare, Foley Urine Collection Kit, Model/Catalog Number: 1555
Hazard: Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
April 29, 2026Medical DevicesFDA
LSL Healthcare Inc. recalls LSL Healthcare, Standard Central Line Dressing Change Kit, Model/Catalog Number: 2717J
Hazard: Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
April 29, 2026Medical DevicesFDA
LSL Healthcare Inc. recalls LSL Healthcare, Central Line Dressing Kit, Model/Catalog Number: 2717H
Hazard: Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.
April 29, 2026Medical DevicesFDA
Foundation Medicine, Inc. recalls Sequencing Agent SEQ0067, component of FoundationOne CDx (F1CDx)
Hazard: Possible increase in phasing, potentially resulting in false-positive BARD1 splice site indel artifact variants
April 29, 2026Medical DevicesFDA
SurgiSmoke Solutions recalls Flamingo Funnel Large, Model Number SQ20012-03
Hazard: Certain lots of product were associated with a manufacturing nonconformance involving use of a non-gamma sterilization compatible drape.
April 29, 2026Medical DevicesFDA
SurgiSmoke Solutions recalls Flamingo Funnel Medium, Model Number SQ20012-02
Hazard: Certain lots of product were associated with a manufacturing nonconformance involving use of a non-gamma sterilization compatible drape.
April 29, 2026Medical DevicesFDA
SurgiSmoke Solutions recalls Flamingo Funnel Small, Model Number SQ20012-01
Hazard: Certain lots of product were associated with a manufacturing nonconformance involving use of a non-gamma sterilization compatible drape.
April 29, 2026Medical DevicesFDA
Remel Europe Ltd. recalls Oxoid Agglutinating Sera, Salmonella 9-0 R30957301
Hazard: Affected lots are not performing to IFU criteria showing cross reactions with 2-0 within 60 seconds. Cross-reactivity may result in the misidentification of a Salmonella 9-O serotype as a 2-O serotype.
April 29, 2026Medical DevicesFDA
Beckman Coulter, Inc. recalls Access Total T4 Calibrator, Catalog No. 33805
Hazard: Beckman Coulter has identified that Access Total T4 Calibrator lots (PN 33805) exhibit a negative bias on DxI 600/800 instruments, with slopes outside product specifications. A false low patient result could cause a patient to undergo unnecessary additional diagnostic testing. A patient may be treated for a disorder not present or receive delayed treatment for hyperthyroidism. For a pregnant patient being monitored for thyroid hormone supplementation, incorrect treatment or dose may be used. A delayed patient results could cause repeat blood draw with associated complications.
April 29, 2026Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls Custom Convenience Kits Pre Op Kit - NS, Part Number AMS14994A
Hazard: The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump administration sets utilized with BBMI s Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump due to potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers or other connections and the ability to prime (occlusion).
April 29, 2026Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls Custom Convenience Kits Pre Op Kit - NS, Part Number AMS14994
Hazard: The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump administration sets utilized with BBMI s Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump due to potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers or other connections and the ability to prime (occlusion).
April 29, 2026Medical DevicesFDA
Windstone Medical Packaging, Inc. recalls Custom Convenience Kits Pre Op Kit - NS, Part Number AMS14433
Hazard: The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump administration sets utilized with BBMI s Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump due to potential for backflow of medication from secondary (piggyback) IV containers into primary IV containers or other connections and the ability to prime (occlusion).
April 29, 2026Medical DevicesFDA
Micro-X Ltd. recalls Rover Mobile X-ray System Model/Catalog Number: MXU-RV35 and MXU-RV71
Hazard: X-Ray generator may malfunction resulting in the X-Ray being inoperable.
April 29, 2026Medical DevicesFDA
ARROW INTERNATIONAL, LLC recalls Arrowg+ard Blue¿ MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters REF ASK-21142-DMC UDI code
Hazard: Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
April 29, 2026Medical DevicesFDA
ARROW INTERNATIONAL, LLC recalls MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters REF ASK-11142-LC2 UDI code: (01)10801902206
Hazard: Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
April 29, 2026Medical DevicesFDA
ARROW INTERNATIONAL, LLC recalls Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC Kit REF ASK-45854-PUPM1 UDI code: (01)10801902159578(17)270531
Hazard: Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
April 29, 2026Medical DevicesFDA
ARROW INTERNATIONAL, LLC recalls ARROW, ARROWG+ARD AND ARROWG+ARD BLUE PLUS PRESSURE INJECTABLE CENTRAL VENOUS CATHETER REF ASK-42802-PLH UDI code:
Hazard: Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
April 29, 2026Medical DevicesFDA
ARROW INTERNATIONAL, LLC recalls FLEXTIP PLUS EPIDURAL CATHETER;FLEXBLOCK CONTINOUS PERIPHERAL NERVE BLOCK CATHETER KIT/SET REF ASK-05502-BSM UDI code:
Hazard: Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
April 29, 2026Medical DevicesFDA
ARROW INTERNATIONAL, LLC recalls PERCUTANEOUS SHEATH INTRODUCER with 7.5 - 8 Fr. Catheter REF ASK-09903-MGH3 UDI code: (01)10801902159127(17)270331(11)2
Hazard: Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
April 29, 2026Medical DevicesFDA
ARROW INTERNATIONAL, LLC recalls ARROW RADIAL ARTERY CATHETERIZATION KIT REF ASK-04220-UCL1 UDI code: (01)10801902159127(17)270331(11)251203(10)33F25J
Hazard: Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured
April 29, 2026Medical DevicesFDA
ARROW INTERNATIONAL, LLC recalls Arrow Echogenic Introducer Needle REF ASK-04001-BWK2 UDI code: (01)10801902220315(17)261231(11)251210(10)33F25J0347
Hazard: Due to receiving a notice from a supplier that the liquid adhesive were incorrectly manufactured
April 29, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2330.
Hazard: Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
April 29, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2138.
Hazard: Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
April 29, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2119.
Hazard: Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
April 29, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2118.
Hazard: Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
April 29, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2117.
Hazard: Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
April 29, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2116.
Hazard: Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
April 29, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2115.
Hazard: XXX
April 29, 2026Medical DevicesFDA
Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2114.
Hazard: Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.