ZOLL Medical Corporation: 7 recalls on record
Recalls filed with 1 agency: FDA (7).
First recall on record: September 26, 2012. Most recent: March 19, 2025.
Risk classification: Class I: 1 · Class II: 6
Most recent recalls
| Date | Agency | Product | Recall number |
|---|---|---|---|
| March 19, 2025 | FDA | Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5S-01C, (2)…Z-1320-2025 | Z-1320-2025 |
| March 19, 2025 | FDA | Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: G5S-80C; Softwa…Z-1321-2025 | Z-1321-2025 |
| July 17, 2024 | FDA | ZOLL Powerheart G5 AED, Semi-Automatic, G5Sxxx Family -Automated external defibrillator (…Z-2324-2024 | Z-2324-2024 |
| June 26, 2024 | FDA | ZOLL 731 Ventilator (EMV+, AEV, Eagle II) - for MRI Compatible Devices - Operator's Guide…Z-2130-2024 | Z-2130-2024 |
| March 21, 2018 | FDA | OneStep CPR Complete, Adult Multi Function Electrodes, Part Numbers: 8900 0214 01 (case o…Z-0977-2018 | Z-0977-2018 |
| April 9, 2014 | FDA | Zoll Medical X Series, PropaqMD, PropaqM Defibrillator/Pacemaker/Monitor With System S…Z-1311-2014 | Z-1311-2014 |
| September 26, 2012 | FDA | Zoll X Series Defibrillator/Pacemaker/Monitor Product Usage: The product is used by q…Z-2401-2012 | Z-2401-2012 |
Questions about this company
- How many recalls does ZOLL Medical Corporation have?
- Recalert has 7 U.S. recalls on record for ZOLL Medical Corporation, published between September 26, 2012 and March 19, 2025.
- What was the most recent ZOLL Medical Corporation recall?
- FDA recall Z-1320-2025, published March 19, 2025: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5S-01C, (2) G5S-02C, (3) G5S-10C, (4) G5S-11C; Software Version: NA Product Description: The Powerheart G5 automated ex…
- Which agencies have handled ZOLL Medical Corporation recalls?
- ZOLL Medical Corporation appears as the recalling firm in recalls from: FDA (7).
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