Reported Jul 17, 2024 · Ongoing

ZOLL Powerheart G5 AED, Semi-Automatic, G5Sxxx Family -Automated external defibrillator (AED) is designed for treating…

Zoll Medical Corporation

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Zoll Medical Corporation · 500 Burdick Pkwy · Deerfield, WI · 53531-9692

Is this the product you have?

ZOLL Powerheart G5 AED, Semi-Automatic, G5Sxxx Family -Automated external defibrillator (AED) is designed for treating life-threatening heart beat irregularities, such as ventricular fibrillation, that cause Sudden Cardiac Arrest (SCA)
Model/Catalog Number
- G5S-00A
- G5S-00A-TSO
- G5S-00C
- G5S-01A
- G5S-02A
- G5S-02C
- G5S-02-L
- G5S-04A
- G5S-05A
- G5S-05C
- G5S-06A
- G5S-06C
- G5S-08A
- G5S-08C
- G5S-10A
- G5S-10C
- G5S-11A
- G5S-11C
- G5S-12C
- G5S-13A
- G5S-14A
- G5S-15A
- G5S-17A
- G5S-17C
- G5S-19A
- G5S-23C
- G5S-29A
- G5S-29C
- G5S-31A
- G5S-31A-SJA
- G5S-31C-SJA
- G5S-36A
- G5S-37A
- G5S-41A
- G5S-41C
- G5S-80A
- G5S-80A-TSO
- G5S-80C
- G5S-80-L
- G5S-82A
- G5S-82C
- G5S-83C
- G5S-90C

Lot codes and dates: GTIN
00812394021239
00812394021277
00812394021284
00812394021413
00812394022779
00847946038182
00847946038199
00847946038243
00847946038250
00847946038304
00847946038328
00847946038335
00847946038342
00847946038359
00847946038380
00847946038397
00847946038403
00847946038410
00847946038434
00847946038441
00847946038496
00847946038519
00847946038533
00847946038571
00847946038588
00847946038663
00847946038816
00847946038830
00847946039028
00847946039035
00847946039066
00847946039127
Serial Number RangeD00000276194-D00000343449
Amount recalled: 14885

Where it was sold

Nationwide
PR
CA
DE
ID
IL
MA
MT

Why it was recalled

G5 Semi-Automatic AED is shipped, with a protective film over its front panel, to protect the screen and shock button from cosmetic damage during shipping. It has come to our attention that customers may not be removing the protective film during deployment of the product. If the protective film is left adhered to the front bezel it may prevent the user from actuating the shock button and may lead to a delay or prevent delivery of defibrillation therapy to a victim suffering from sudden cardiac arrest

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Zoll Medical Corporation recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.

By hazard

Medical device recalls

Other recalls from Zoll Medical Corporation

7 in total.

Where it was distributed

All recall categories · Browse the whole archive