Philips North America Llc: 179 recalls on record
Recalls filed with 1 agency: FDA (179).
First recall on record: April 5, 2017. Most recent: September 9, 2026.
Risk classification: Class I: 5 · Class II: 174
Most recent recalls
| Date | Agency | Product | Recall number |
|---|---|---|---|
| April 3, 2019 | FDA | MultiDiagnost-Eleva, Product codes 708032, 708036 Product Usage: As a multifunctional…Z-1052-2019 | Z-1052-2019 |
| February 27, 2019 | FDA | PageWriter TC50, Product 860310, Software revisions up to and including A.07.05.22 used t…Z-0854-2019 | Z-0854-2019 |
| February 27, 2019 | FDA | PageWriter TC70, Product 860315, Software revisions up to and including A.07.05.22 used t…Z-0853-2019 | Z-0853-2019 |
| April 5, 2017 | FDA | HeartStart MRx Monitor/Defibrillator, Model numbers: M3535A (M3535ATZ) M3536A (M3536ATZ)…Z-1417-2017 | Z-1417-2017 |
Questions about this company
- How many recalls does Philips North America Llc have?
- Recalert has 179 U.S. recalls on record for Philips North America Llc, published between April 5, 2017 and September 9, 2026.
- Which agencies have handled Philips North America Llc recalls?
- Philips North America Llc appears as the recalling firm in recalls from: FDA (179).
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