Every recall we track for CME America, LLC — 47 in all — plus the complaints and injury reports the public filed about them.
CME America recalls T34L syringe pumps with serial numbers starting 26294-70196 due to potential under infusion without alarm or pump damage from cleaning fluid. Affected users should check their serial numbers and contact CME America for details.
CME America recalls NeoThrive T-Syr: pumps may under-infuse medications without alarm due to motor wear or cracks. Affected models include 100-101PSL. Stop using immediately to prevent medication errors.
CME America recalls Ameritus 1st Enteral Pump due to potential under infusion without alarm. Check serial numbers listed to see if your pump is affected.
CME America recalls T-Syringe Pump Neofeed models with potential under infusion without pump alarm due to motor wear or cracks. Affected units have specific serial numbers and UDI codes.
CME America recalls T34L PCA syringe pumps with serial numbers 26484-26486 and UDI code B101100106PSL0 due to risk of under infusion without pump alarm. Affected users should contact CME America for details.
CME America recalls T34 T-Syringe Pump models with serial numbers 58771-58999 and others due to pump motor block mechanism wear causing under infusion without alarm. This may lead to medication underdosing.
CME America recalls BodyGuard Microset infusion sets with potential delivery inaccuracies of up to 17.5% over therapy. Affected units may cause over or under infusion of medication.
CME America recalls CMExpress Microbore Sets (REF: A120-160CYFRV) due to potential delivery inaccuracy of up to 17.5% in infusion therapy, risking over or under-dosing.
CME America recalls BodyGuard Microset (REF: A100-163XES) due to potential infusion delivery inaccuracies that could cause over or under therapy. All lots within expiry date are affected.
CME America recalls BodyGuard Microset (A120-125XSE) due to potential infusion delivery inaccuracies that could cause over or under therapy. Affected units include all lots within expiry.
CME America recalls CMExpress Microbore Sets (REF: A120-160C2YRV) due to potential delivery inaccuracies of up to 17.5% in infusion therapy, risking over or under-dosing.
CME America recalls CMExpress Microbore Set (REF: A120-161CYF) due to potential delivery inaccuracies in infusion therapy, risking over or under-dosing of medication.
CME America recalls BodyGuard Microset (A100-163XSFL) due to potential infusion delivery inaccuracies that could cause over or under therapy. All lots within expiry are affected.
CME America recalls BodyGuard Microset (REF: A12:161XYB) due to potential infusion delivery inaccuracies that could cause over or under therapy. Affected units include all lots within expiry date.
CME America recalls CMExpress Needleless Y Site Microb: sets with delivery inaccuracy over 13% that could cause over or under infusion of therapy. Affected units include all lots within expiry.
CME America recalls BodyGuard Microset (REF: A12:160GCFA) due to potential infusion delivery inaccuracies that could cause over or under therapy. Affected units include all lots within expiry.
CME America recalls BodyGuard Microset infusion sets with potential delivery inaccuracies of up to 13% over/under, risking incorrect therapy dosing. Affected units include all lots within expiry date.
CME America recalls BodyGuard Microset with Needleless Adaptor (REF: A12:003XSNY) due to potential infusion delivery inaccuracies that could cause over or under therapy. Affected units may need replacement.
CME America recalls CMExpress Microbore Set (REF: A120-160CRV) due to potential infusion delivery inaccuracies of up to 17.5% over therapy, risking over or under-dosing.
CME America recalls CMExpress Microbore Set (REF: A120-160C) for potential infusion delivery inaccuracies that could cause over- or under-infusion of therapy.
CME America recalls BodyGuard Microset with Filter (REF: A100-163XESF) due to potential infusion delivery inaccuracies that could cause over or under therapy. Affected units include all lots within expiry.
CME America recalls BodyGuard Microset infusion sets with potential delivery inaccuracies of up to 17.5% over therapy. Affected units may cause over or under-infusion of medication.
CME America recalls BodyGuard Microset infusion sets with potential delivery inaccuracy of up to 17.5% over therapy, risking over or under-infusion. Affected units include all lots within expiry date.
CME America recalls BodyGuard Microset infusion sets with potential delivery inaccuracy of up to 17.5% over therapy, risking over or under-infusion of medication.
CME America recalls BodyGuard Microset infusion sets with potential delivery inaccuracy of up to 17.5% over therapy, risking over or under-infusion. Affected units include specific model and all lots within expiry.
CME America recalls BodyGuard Microset infusion sets with potential delivery inaccuracies of up to 17.5% over therapy, risking over or under-infusion of medication.
CME America recalls BodyGuard Microset infusion sets with potential delivery inaccuracy of up to 17.5% over therapy, risking over or under-infusion of medication.
CME America recalls BodyGuard Microset with Filter (REF: A100-164XESF) due to potential infusion delivery inaccuracies that could cause over or under therapy. All lots within expiry are affected.
CME America recalls BodyGuard Microset with Male Luer Connectors (REF A100-163XEBF) due to potential infusion delivery inaccuracies that could cause over or under therapy administration.
CME America recalls Standard BodySet with Needleless Connectors (REF: A120-125XS) due to potential infusion accuracy issues that could cause over or under delivery of therapy.
CME America recalls BodyGuard Microset infusion sets with potential delivery inaccuracy of up to 17.5% over therapy, risking over or under-infusion of medication.
CME America recalls BodyGuard Microset infusion sets with potential delivery inaccuracies of up to 17.5% over/under therapy. Affected units may cause over or under infusion of medication.
CME America recalls BodyGuard Microset infusion sets with potential delivery inaccuracies (up to 17.5% over/under) that could cause unsafe therapy dosing. Affected units include all lots within expiry date.
CME America recalls BodyGuard Microset with Filter and Manual Priming Valve (REF: A12:112XSFV) due to potential infusion delivery inaccuracies that could cause over or under therapy administration.
CME America recalls BodyGuard Microset with Filter (REF: A12:0-160XSFE) due to potential infusion delivery inaccuracies that could cause over- or under-infusion of therapy.
CME America recalls BodyGuard infusion sets with Female Luer (REF A12:003XSN) due to potential delivery inaccuracies of up to 17.5% over therapy doses, risking over or under-infusion.
CME America recalls BodyGuard Microset infusion sets with potential delivery inaccuracies up to 17.5% over/under therapy. Affected units may cause over or under-infusion of medication.
CME America recalls CMExpress Microbore Sets (REF: A120-161C) due to potential delivery inaccuracies causing over or under infusion of therapy. All lots within expiry are affected.
CME America recalls BodyGuard Microset infusion sets with potential delivery inaccuracies of up to 17.5% over/under therapy. Affected units may cause over or under infusion of medication.
CME America recalls BodyGuard BodySet (REF: A12:0-160SAS) due to potential infusion delivery inaccuracies that could cause over or under therapy. Affected units include all lots within expiry date.
CME America recalls BodyGuard Microset infusion sets with potential delivery inaccuracy of up to 17.5% over therapy, risking over or under-infusion. Affected units include all lots within expiry.
CME America recalls BodyGuard Microset With Female Luer (REF: A12:160XPSN) due to potential infusion delivery inaccuracies that could cause over or under therapy. Affected units may need replacement.
CME America recalls BodyGuard Microset (REF: A12:161XPS) due to potential infusion delivery inaccuracies that could cause over or under therapy. Affected units include all lots within expiry date.
CME America recalls BodyGuard Wall Charger (Lot 2019-0364) due to risk of improper infusion pump battery charging. Affected units may not charge correctly, potentially causing medical issues.
CME America recalls BodyGuard Microset tubing with potential incorrect filter pore size that could affect medication delivery safety.
CME America recalls BodyGuard infusion pumps (BG 323, BG 121, etc.) due to potential 13% delivery inaccuracy at low/high flow rates. Affected units may deliver drugs too fast or too slow, risking treatment errors.
CME America recalls BodyGuard Microset tubing (REF A120-003XYVA) due to potential under-delivery of fluids when used with infusion pumps. Affected units include specific lot numbers.
