Severity
Moderate
FDA Drug recall · Reported May 14, 2014
Microbial Contamination of Non-Sterile Products: Elevated counts of bacteria was found, Serratia liquefaciens.
The recall
Mangiacotti issued this moderate-severity FDA Drug recall — Microbial Contamination of Non-Sterile Products: Elevated counts of bacteria was found, Serratia liquefacien….
Sourced from official FDA Drug enforcement records. Verify recall #D-1306-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Drug action (record #D-1306-2014) was formally reported on May 14, 2014, with the manufacturer initiating the action on December 27, 2013. It is classified under Moderate severity (Class II), with a current status of Terminated. Mangiacotti is listed as the recalling firm, operating out of Attleboro, MA. Federal records indicate N/A units are affected.
The documented reason for this recall is: Microbial Contamination of Non-Sterile Products: Elevated counts of bacteria was found, Serratia liquefaciens. Distribution data in the federal record shows the product reached: Nationwide. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC and NHTSA going back to 1995. Within the same product category, the database holds 6 closely related recalls. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 12 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.
Of 83,949 recalls in the database, 21,198 are high severity, 58,883 moderate, and 3,868 low. This recall is classified moderate severity.
Severity
Moderate
Units Affected
N/A
Related Recalls
6
0 from same agency
Mangiacotti - Clementine Hand Sanitizer Spray, alcohol free, 0.5 fl Oz. 15 mL spray bottle, UPC 870678005337, Active Ingredient Benzalkonium Chloride 0.1%, Dist By: Mangiacotti, Attleboro, MA 02703.
Microbial Contamination of Non-Sterile Products: Elevated counts of bacteria was found, Serratia liquefaciens.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | D-1306-2014 |
| Date reported | May 14, 2014 |
| Date initiated | December 27, 2013 |
| Recalling firm | Mangiacotti |
| Units affected | N/A |
| Distribution | Nationwide |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
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Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Drug, reported May 14, 2014.
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.
Read our methodology — how this data is sourced, computed, and verified.
Source: Federal recall agencies (FDA, CPSC, NHTSA) Aggregated federal recall feeds Recall data normalized across FDA, CPSC and NHTSA feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type).