Severity
Low
LowClass IIITerminated
FDA Drug recall · Reported August 7, 2019
TOOTSIE ROLL FRUIT CHEWS LIME SCENTED ANTIBACTERIAL HAND GEL (Ethyl Alcohol 62%), 1.35 fl oz / 40 mL, OTC, Distributed by: JFL Enterprises, Inc. Cleveland, Ohio 44102.
CGMP deviations: Stability testing was not conducted on manufactured sunscreen and hand sanitizer OTC products.
NingBo Huize Commodity Co.,Ltd. recalled TOOTSIE ROLL FRUIT CHEWS LIME SCENTED ANTIBACTERIAL HAND GEL (Ethyl Alcohol 62%), 1.35 fl… - a low-severity action.
TOOTSIE ROLL FRUIT CHEWS LIME SCENTED ANTIBACTERIAL HAND GEL (Ethyl Alcohol 62%), 1.35 fl… was recalled by NingBo Huize Commodity Co.,Ltd. in August 7, 2019. Reason: CGMP deviations: Stability testing was not conducted on manufactured sunscreen and hand sanitizer OTC product…. Check the official notice for the remedy. Verify recall #D-1550-2019 with the FDA Drug before acting.
The recall
NingBo Huize Commodity Co.,Ltd. issued this low-severity FDA Drug recall-CGMP deviations: Stability testing was not conducted on manufactured sunscreen and hand sanitizer OTC product….
- Low
- severity level
- 9K units
- affected scope
- Class III
- classification
- August 7, 2019
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-1550-2019 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-1550-2019) was formally reported on August 7, 2019, with the manufacturer initiating the action on April 1, 2019. It is classified under Low severity (Class III), with a current status of Terminated. NingBo Huize Commodity Co.,Ltd. is listed as the recalling firm, operating out of Yuyao, N/A. Federal records list the affected scope as 8,856.
The documented reason for this recall is: CGMP deviations: Stability testing was not conducted on manufactured sunscreen and hand sanitizer OTC products. Distribution data in the federal record shows the product reached: Foreign manufacturer located in China and distributed to seven consignees located in China.. 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 - 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.
Food recalls over time
Where this recall sits in its category - 25,126 food 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
8,856
Related Recalls
6
0 from same agency
Product description
TOOTSIE ROLL FRUIT CHEWS LIME SCENTED ANTIBACTERIAL HAND GEL (Ethyl Alcohol 62%), 1.35 fl oz / 40 mL, OTC, Distributed by: JFL Enterprises, Inc. Cleveland, Ohio 44102.
Reason for recall
CGMP deviations: Stability testing was not conducted on manufactured sunscreen and hand sanitizer OTC products.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | D-1550-2019 |
| Date reported | August 7, 2019 |
| Date initiated | April 1, 2019 |
| Recalling firm | NingBo Huize Commodity Co.,Ltd. |
| Firm location | Yuyao, N/A |
| Affected scope | 8,856 |
| Distribution | Foreign manufacturer located in China and distributed to seven consignees located in China. |
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-1550-2019) 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.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. 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? ▼
TOOTSIE ROLL FRUIT CHEWS LIME SCENTED ANTIBACTERIAL HAND GEL (Ethyl Alcohol 62%), 1.35 fl oz / 40 mL, OTC, Distributed by: JFL Enterprises, Inc. Cleveland, Ohio 44102.. Recalled by NingBo Huize Commodity Co.,Ltd.. Units affected: 8,856.
Why was this product recalled? ▼
CGMP deviations: Stability testing was not conducted on manufactured sunscreen and hand sanitizer OTC products.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on August 7, 2019. Severity: Low. Recall number: D-1550-2019.
Where was the recalled product distributed? ▼
Distribution: Foreign manufacturer located in China and distributed to seven consignees located in China..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-1550-2019) 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.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Compare this recall with Conair Recalls Over One Million Cuisinart Grill Brushes Due… →
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 Drug, reported August 7, 2019. 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.