Exact FDA event identifier

Event 68616

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

Event summary

Timeline bucket: May 30, 2014
Product types: Drug
Classifications: Class II
Statuses: Terminated
Recalling firm wording: Brookfield Prescription Center Inc. dba MD Custom Rx

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

6 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 6

Mometasone 0.6 mg /60 mL Irrigation solution, 4000 mL bottle, Rx only, MD Custom Rx, 19035 W. Capitol Dr., Ste. 105, Brookfield, WI 53045

D-1416-2014

Recall number: D-1416-2014
Initiated: May 30, 2014
Classification: Class II
Status: Terminated
Recalling firm: Brookfield Prescription Center Inc. dba MD Custom Rx
Quantity: 6000 mL

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Incorrect/Undeclared Excipients: Specific drug products were compounded with an incorrect solvent.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Incorrect/Undeclared Excipients: Specific drug products were compounded with an incorrect solvent.

Code information

Lot # / Beyond Use Date: 04282014@11 / BUD 05/28/14; 04212014@4 / BUD 05/21/2014

Distribution pattern

WI only

drug · product 2 of 6

Diphenhydramine (Alcohol Base) 25 mg / 0.5 mL Solution, 30 mL bottle, Rx only, MD Custom Rx, 19035 W. Capitol Dr., Ste. 105, Brookfield, WI 53045

D-1417-2014

Recall number: D-1417-2014
Initiated: May 30, 2014
Classification: Class II
Status: Terminated
Recalling firm: Brookfield Prescription Center Inc. dba MD Custom Rx
Quantity: 30 mL

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Incorrect/Undeclared Excipients: Specific drug products were compounded with an incorrect solvent.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Incorrect/Undeclared Excipients: Specific drug products were compounded with an incorrect solvent.

Code information

Lot # / Beyond Use Date: 05012014@36 / 05/15/14

Distribution pattern

WI only

drug · product 3 of 6

HCG (Human Chorionic Gonadotropin) 125 units/ 0.1 mL drop, 5 mL bottle, Rx only, MD Custom Rx, 19035 W. Capitol Dr., Ste. 105, Brookfield, WI 53045

D-1418-2014

Recall number: D-1418-2014
Initiated: May 30, 2014
Classification: Class II
Status: Terminated
Recalling firm: Brookfield Prescription Center Inc. dba MD Custom Rx
Quantity: 184 mL

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Incorrect/Undeclared Excipients: Specific drug products were compounded with an incorrect solvent.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Incorrect/Undeclared Excipients: Specific drug products were compounded with an incorrect solvent.

Code information

Lot # / Beyond Use Date: 05192014@15 / BUD 07/18/14; 04142014@39 / BUD 6-13-14; 04182014@4 / BUD 6-17-14; 04162014@12 / BUD 06/15/14; 05092014@34 / BUD 07/08/14; 04162014@35 / BUD 06/15/14; 05232014@33 / BUD 07/22/14; 05022014@36 / BUD 7/1/14; 04292014@13 / BUD 06/28/14; 04282014@43 / BUD 06/27/14; 05212014@5 / BUD 07/20/14; 04292014@13 / BUD 06/28/14; 05062014@42 / BUD 07/05/14; 05022014@36 / BUD 07/01/14; 05062014@45 / BUD 07/05/14; 05082014@2 / BUD 07/07/14, 05152014@36 / BUD 7/14/14; 05212014@5 / BUD 07/20/14; 05082014@2 / BUD 07/07/14; 05132014@37 / BUD 07/12/14; 05082014@2 / BUD 07/07/14; 05132014@38 / BUD 07/12/14; 04242014@14 / BUD 6-23-14; 04162014@12 / BUD 6-15-14; 04212014@27 / BUD 6-20-14; 04292014@13 / BUD 6-28-14; 05092014@34 / BUD 7-8-14; 05212014@5 / BUD 7-20-14; 05272014@58 / BUD 7-26-14; 05222014@27 / BUD 07/21/14

Distribution pattern

WI only

drug · product 4 of 6

HCG 125U/Tab Tablet Tritu, 50 tablets per bottle, Rx only, MD Custom Rx, 19035 W. Capitol Dr., Ste. 105, Brookfield, WI 53045

D-1419-2014

Recall number: D-1419-2014
Initiated: May 30, 2014
Classification: Class II
Status: Terminated
Recalling firm: Brookfield Prescription Center Inc. dba MD Custom Rx
Quantity: 850 tablets

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Incorrect/Undeclared Excipients: Specific drug products were compounded with an incorrect solvent.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Incorrect/Undeclared Excipients: Specific drug products were compounded with an incorrect solvent.

Code information

Lot # / Beyond Use Date: 05022014@5 / BUD 07/01/14; 04032014@7 / BUD 06/02/14; 04092014@16 / BUD06/08/14; 04142014@51 / BUD 06-13-14; 04152014@48 / BUD 06/14/14; 04172014@42 / BUD 06-06-14; 04182014@45 / BUD 6-17-14; 05162014@41 / BUD 07/15/14; 04172014@44 / BUD 06/16/14; 04212014@37 / BUD 6/20/14; 04222014@10 / BUD 06/21/14; 04232014@30 / BUD 06/22/14; 05072014@37 / BUD 07-06-14; 04292014@31 / BUD 06/28/14; 04302014@9 / BUD 06/29/14; 04252014@43 / BUD 06/24/14; 04222014@28 / BUD 6 -21-14

Distribution pattern

WI only

drug · product 5 of 6

HCG (Human Chorionic Gonadotropin) 200 units/ 0.1 mL drops, packaged in 5 mL and 10 mL bottles, Rx only, MD Custom Rx, 19035 W. Capitol Dr., Ste. 105, Brookfield, WI 53045

D-1420-2014

Recall number: D-1420-2014
Initiated: May 30, 2014
Classification: Class II
Status: Terminated
Recalling firm: Brookfield Prescription Center Inc. dba MD Custom Rx
Quantity: 55 mL

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Incorrect/Undeclared Excipients: Specific drug products were compounded with an incorrect solvent.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Incorrect/Undeclared Excipients: Specific drug products were compounded with an incorrect solvent.

Code information

Lot # / Beyond Use Date: 04232014@49 / BUD 06-22-14; 04232014@2 / BUD 06/22/14; 04252014@27 / BUD 06/24/14; 04162014@33 / BUD06/15/14; 05132014@2 / BUD 07/12/14; 05092014@39 BUD 7-8-14

Distribution pattern

WI only

drug · product 6 of 6

HCG (Human Chorionic Gonadotropin) + Methylcobalamin (Methyl B12), 1500 units + 1000 mcg/mL drop, 8 mL bottle, Rx only, MD Custom Rx, 19035 W. Capitol Dr., Ste. 105, Brookfield, WI 53045

D-1421-2014

Recall number: D-1421-2014
Initiated: May 30, 2014
Classification: Class II
Status: Terminated
Recalling firm: Brookfield Prescription Center Inc. dba MD Custom Rx
Quantity: 8 mL

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Incorrect/Undeclared Excipients: Specific drug products were compounded with an incorrect solvent.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Incorrect/Undeclared Excipients: Specific drug products were compounded with an incorrect solvent.

Code information

Lot # / Beyond Use Date: 04302014@21 / BUD 06/29/14

Distribution pattern

WI only