Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported April 16, 2014
Playtex Nurser Deluxe Double Electric Breast Pump, Model X06578AO, powered by a 12V DC power supply, Model SY-12120, which is included with the package.
Some of the power adapters outer casings may become loose and separate, resulting in a potential for electric shock.
Energizer Personal Care recalled Playtex Nurser Deluxe Double Electric Breast Pump, Model X06578AO, powered by a 12V DC po… - a moderate-severity action.
Playtex Nurser Deluxe Double Electric Breast Pump, Model X06578AO, powered by a 12V DC po… was recalled by Energizer Personal Care in April 16, 2014. Reason: Some of the power adapters outer casings may become loose and separate, resulting in a potential for electric…. Check the official notice for the remedy. Verify recall #Z-1336-2014 with the FDA Devices before acting.
The recall
Energizer Personal Care issued this moderate-severity FDA Devices recall-Some of the power adapters outer casings may become loose and separate, resulting in a potential for electric….
- Moderate
- severity level
- 36K units
- affected scope
- Class II
- classification
- April 16, 2014
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-1336-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-1336-2014) was formally reported on April 16, 2014, with the manufacturer initiating the action on March 18, 2014. It is classified under Moderate severity (Class II), with a current status of Terminated. Energizer Personal Care is listed as the recalling firm, operating out of Shelton, CT. Federal records list the affected scope as 35,803.
The documented reason for this recall is: Some of the power adapters outer casings may become loose and separate, resulting in a potential for electric shock. Distribution data in the federal record shows the product reached: USA Nationwide Distribution in the states of: AL, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, KY, MD, MI, MN, MO, NC, NJ, NV, NY, OH, ON, OR, PA, SC, TN, TX, VA, VT, WA, WI Canada - one consignee, Energizer (recalling…. 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 moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
35,803
Related Recalls
6
3 from same agency
Product description
Playtex Nurser Deluxe Double Electric Breast Pump, Model X06578AO, powered by a 12V DC power supply, Model SY-12120, which is included with the package.
Reason for recall
Some of the power adapters outer casings may become loose and separate, resulting in a potential for electric shock.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-1336-2014 |
| Date reported | April 16, 2014 |
| Date initiated | March 18, 2014 |
| Recalling firm | Energizer Personal Care |
| Firm location | Shelton, CT |
| Affected scope | 35,803 |
| Distribution | USA Nationwide Distribution in the states of: AL, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, KY, MD, MI, MN, MO, NC, NJ, NV, NY, OH, ON, OR, PA, SC, TN, TX, VA, VT, WA, WI Canada - one consignee, Energizer (recalling firm's) company sto… |
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-1336-2014) 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? ▼
Playtex Nurser Deluxe Double Electric Breast Pump, Model X06578AO, powered by a 12V DC power supply, Model SY-12120, which is included with the package.. Recalled by Energizer Personal Care. Units affected: 35,803.
Why was this product recalled? ▼
Some of the power adapters outer casings may become loose and separate, resulting in a potential for electric shock.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 16, 2014. Severity: Moderate. Recall number: Z-1336-2014.
Where was the recalled product distributed? ▼
Distribution: USA Nationwide Distribution in the states of: AL, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, KY, MD, MI, MN, MO, NC, NJ, NV, NY, OH, ON, OR, PA, SC, TN, TX, VA, VT, WA, WI Canada - one consignee, Energizer (recalling firm's) company store.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-1336-2014) 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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Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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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 April 16, 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.