Severity
Low
LowClass IIITerminated
FDA Devices recall · Reported July 30, 2014
Zoll Circulation LifeBand Single Pack (accessory), and Nickel-metal hydride (NIMH) Battery. The LifeBand is a chest compression assembly that consists of a cover plate and two bands integrated with a compression pad with a Velcro fastener. The AutoPulse Battery is a removable component that supplies power for the AutoPulse operation. Used in the AutoPulse Resuscitation System Model 100, for chest compressions as an adjunct to manual CPR.
Typographical error in the Japanese legal label of the AutoPulse Resuscitation System Model 100. The label is specific to the Japanese version of the product.
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Zoll Circulation, Inc. recalled Zoll Circulation LifeBand Single Pack (accessory), and Nickel-metal hydride (NIMH) Batter… - a low-severity action.
Zoll Circulation LifeBand Single Pack (accessory), and Nickel-metal hydride (NIMH) Batter… was recalled by Zoll Circulation, Inc. in July 30, 2014. Reason: Typographical error in the Japanese legal label of the AutoPulse Resuscitation System Model 100. The label is…. Check the official notice for the remedy. Verify recall #Z-2090-2014 with the FDA Devices before acting.
The recall
Zoll Circulation, Inc. issued this low-severity FDA Devices recall-Typographical error in the Japanese legal label of the AutoPulse Resuscitation System Model 100. The label is….
- Low
- severity level
- Class III
- classification
- July 30, 2014
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-2090-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-2090-2014) was formally reported on July 30, 2014, with the manufacturer initiating the action on July 16, 2013. It is classified under Low severity (Class III), with a current status of Terminated. Zoll Circulation, Inc. is listed as the recalling firm, operating out of San Jose, CA. Federal records list the affected scope as 161 Nickel Metal batteries, 40 LifeBand.
The documented reason for this recall is: Typographical error in the Japanese legal label of the AutoPulse Resuscitation System Model 100. The label is specific to the Japanese version of the product. Distribution data in the federal record shows the product reached: Distributed in Japan.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
161 Nickel Metal batteries, 40 LifeBand
Related Recalls
6
3 from same agency
Product description
Zoll Circulation LifeBand Single Pack (accessory), and Nickel-metal hydride (NIMH) Battery. The LifeBand is a chest compression assembly that consists of a cover plate and two bands integrated with a compression pad with a Velcro fastener. The AutoPulse Battery is a removable component that supplies power for the AutoPulse operation. Used in the AutoPulse Resuscitation System Model 100, for chest compressions as an adjunct to manual CPR.
Reason for recall
Typographical error in the Japanese legal label of the AutoPulse Resuscitation System Model 100. The label is specific to the Japanese version of the product.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | Z-2090-2014 |
| Date reported | July 30, 2014 |
| Date initiated | July 16, 2013 |
| Recalling firm | Zoll Circulation, Inc. |
| Firm location | San Jose, CA |
| Affected scope | 161 Nickel Metal batteries, 40 LifeBand |
| Distribution | Distributed in Japan. |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-2090-2014) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Zoll Circulation LifeBand Single Pack (accessory), and Nickel-metal hydride (NIMH) Battery. The LifeBand is a chest compression assembly that consists of a cover plate and two bands integrated with a compression pad with a Velcro fastener. The AutoPulse Battery is a removable component that supplies power for the AutoPulse operation. Used in the AutoPulse Resuscitation System Model 100, for chest compressions as an adjunct to manual CPR.. Recalled by Zoll Circulation, Inc.. Units affected: 161 Nickel Metal batteries, 40 LifeBand.
Why was this product recalled? ▼
Typographical error in the Japanese legal label of the AutoPulse Resuscitation System Model 100. The label is specific to the Japanese version of the product.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 30, 2014. Severity: Low. Recall number: Z-2090-2014.
Where was the recalled product distributed? ▼
Distribution: Distributed in Japan..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-2090-2014) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported July 30, 2014. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.