Severity
Critical
CriticalClass ITerminated
FDA Drug recall · Reported February 22, 2017
SLIMFIT X capsules, packaged in a 60-cont bottle
Marketed without an approved NDA/ANDA: Product contains undeclared sibutramine and desmethylsibutramine.
Jersey Shore Supplements, LLC recalled SLIMFIT X capsules, packaged in a 60-cont bottle — a critical-severity action.
SLIMFIT X capsules, packaged in a 60-cont bottle was recalled by Jersey Shore Supplements, LLC in February 22, 2017. Reason: Marketed without an approved NDA/ANDA: Product contains undeclared sibutramine and desmethylsibutramine.. Check the official notice for the remedy. Verify recall #D-0473-2017 with the FDA Drug before acting.
The recall
Jersey Shore Supplements, LLC issued this critical-severity FDA Drug recall — Marketed without an approved NDA/ANDA: Product contains undeclared sibutramine and desmethylsibutramine..
- Critical
- severity level
- Class I
- classification
- February 22, 2017
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0473-2017 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0473-2017) was formally reported on February 22, 2017, with the manufacturer initiating the action on December 9, 2016. It is classified under Critical severity (Class I), with a current status of Terminated. Jersey Shore Supplements, LLC is listed as the recalling firm, operating out of Bradley Beach, NJ. Federal records list the affected scope as 150 bottles.
The documented reason for this recall is: Marketed without an approved NDA/ANDA: Product contains undeclared sibutramine and desmethylsibutramine. Distribution data in the federal record shows the product reached: New Jersey and Maryland.. 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, 5 from FDA Drug — 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.
Drugs & Medications recalls over time
Where this recall sits in its category — 14,048 drugs & medications recalls on record
Where this recall sits in the database
Of 100,165 recalls in the database, 23,668 are high severity, 72,097 moderate, and 4,400 low. This recall is classified high severity.
Counts reflect market size and reporting activity, not inherent danger — we do not rank products by risk from raw recall volume.
Affected scope
150 bottles
Related Recalls
6
5 from same agency
Product description
SLIMFIT X capsules, packaged in a 60-cont bottle
Reason for recall
Marketed without an approved NDA/ANDA: Product contains undeclared sibutramine and desmethylsibutramine.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Terminated |
| Recall number | D-0473-2017 |
| Date reported | February 22, 2017 |
| Date initiated | December 9, 2016 |
| Recalling firm | Jersey Shore Supplements, LLC |
| Firm location | Bradley Beach, NJ |
| Affected scope | 150 bottles |
| Distribution | New Jersey and Maryland. |
Profile values are sourced directly from the official FDA Drug 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 (D-0473-2017) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug before acting — recall details can be updated.
- This is a Class I (high-risk) recall — stop using the product immediately and follow the disposal or return instructions. What to do next
This page summarizes the official FDA Drug 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? ▼
SLIMFIT X capsules, packaged in a 60-cont bottle. Recalled by Jersey Shore Supplements, LLC. Units affected: 150 bottles.
Why was this product recalled? ▼
Marketed without an approved NDA/ANDA: Product contains undeclared sibutramine and desmethylsibutramine.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on February 22, 2017. Severity: Critical. Recall number: D-0473-2017.
Where was the recalled product distributed? ▼
Distribution: New Jersey and Maryland..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-0473-2017) against your product. Visit the official FDA Drug 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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What to do next
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Data Sources
Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Drug, reported February 22, 2017.
- Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
- Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
- Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records — no number is typed in by an editor. 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 June 2026.