Smiths Medical recalls Palm Cups (model 55-4090) due to possible incorrect shipping labels. This could lead to confusion during use for chest percussion. No immediate action needed as the hazard is low risk.
The firm became aware via complaints that one lot of ACE MDI Spacers with Small Masks and one lot of Palm Cups (Large) may have incorrect shipping box labels.
Smiths Medical is recalling Palm Cups (model 55-1090) because some units may have incorrect shipping labels. This could cause confusion when using the device for chest percussion, but the hazard is low risk and no action is required.
Incorrect shipping labels could lead to confusion about which units are being used. This might cause improper use if the wrong model is selected, but the hazard is low risk as the device itself is safe.
Healthcare professionals using the Palm Cups for chest percussion therapy may be affected. Those most at risk are users who rely on accurate labeling for proper device use.
Check for the model number 55-4090 on the Palm Cups. The lot number 3768545 is associated with the affected units. The product was sold with incorrect shipping labels in specific lots.
Verify the model number and lot number on the Palm Cups to determine if they are affected.
No, the recall does not require stopping use. The hazard is low risk and no action is needed.
Check the model number and lot number on your Palm Cups. If they match the affected units, no action is required as the hazard is low risk.
The recall addresses potential confusion from incorrect labels, but there is no risk of injury as the hazard is low risk.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1515-2021 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-1515-2021 from Smiths Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
