Exact FDA event identifier

Event 64640

2 recalled-product records grouped only because every row carries this exact official event ID.

Event summary

Timeline bucket: March 14, 2013
Product types: Drug
Classifications: Class I and Class II
Statuses: Terminated
Recalling firm wording: Med Prep Consulting, Inc.

Dossier provenance

Source snapshots represented here

openFDA Drug Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Device root-cause evidence is not applicable to this event. No grouped product has the official product type device; this is not an unavailable-enrichment finding.

Complete imported group

Every recalled product in this event

2 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

drug · product 1 of 2

Magnesium Sulfate 2 grams in Dextrose 5% for Injection, in 50 mL Plastic Infusion Bags, Med Prep Consulting Inc., Tinton Falls, NJ 07712

D-810-2013

Recall number: D-810-2013
Initiated: March 14, 2013
Classification: Class I
Status: Terminated
Recalling firm: Med Prep Consulting, Inc.
Quantity: 403883 bags

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0

mold contamination

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Non-Sterility; mold contamination

Code information

All lots

Distribution pattern

Press States Nationwide. Distribution List indicates the following: DE, FL, IL, IN, ME, MI, NJ, PA, TX, and VA

drug · product 2 of 2

All Compounded Products, packaged in plastic infusion bags, devices, syringes and glass vials, Med Prep Consulting Inc., Tinton Falls, NJ 07712

D-811-2013

Recall number: D-811-2013
Initiated: March 14, 2013
Classification: Class II
Status: Terminated
Recalling firm: Med Prep Consulting, Inc.
Quantity: N/A

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0

mold contamination

Sterility assurance reason.sterility_assurance · v1.0.0

Lack of Assurance of Sterility

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Lack of Assurance of Sterility; potential for mold contamination

Code information

All lots

Distribution pattern

Press States Nationwide. Distribution List indicates the following: DE, FL, IL, IN, ME, MI, NJ, PA, TX, and VA