Recall events
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Event 82615
Event summary
Timeline bucket April 08, 2019
Product types Drug
Classifications Class II
Statuses Terminated
Recalling firm wording Customceutical Compounding
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
10 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 10
BPlex (METHYLCOBALAMIN 1000 MCG/ML PYRIDOXAL 5 PHOSPHATE 20MG/ML DEXPANTHENOL 250MG/ML), 10 ML MULTIDOSE VIAL MDV INJ COMPOUNDED. Customceutical Compounding 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028 Ph. 480 516 0272
D-1253-2019
Recall number D-1253-2019
Initiated April 08, 2019
Classification Class II
Status Terminated
Quantity 32 vials
App-derived interpretation
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 for injectables and solutions intended to be sterile.
Code information Lot #: 02082019@9, Exp 5/19/19
Distribution pattern U.S.A. Nationwide
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[11195]
FDA event record
· Exact recall-number query on openFDA
drug · product 2 of 10
BPlex (METHYLCOBALAMIN 1000 MCG/ML PYRIDOXAL 5 PHOSPHATE 20MG/ML DEXPANTHENOL 250MG/ML), 10 ML MULTIDOSE VIAL MDV INJ COMPOUNDED. Customceutical Compounding 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028 Ph. 480 516 0272
D-1254-2019
Recall number D-1254-2019
Initiated April 08, 2019
Classification Class II
Status Terminated
Quantity 19 vials
App-derived interpretation
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 for injectables and solutions intended to be sterile.
Code information Lot #: 03122019@31, Exp 6/10/19
Distribution pattern U.S.A. Nationwide
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[11371]
FDA event record
· Exact recall-number query on openFDA
drug · product 3 of 10
Glutathione 200mg/mL inj. a) 10 ML and b) 12 ML MULTIDOSE VIAL MDV Compounded. Customceutical Compounding 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028 Ph. 480 516 0272
D-1255-2019
Recall number D-1255-2019
Initiated April 08, 2019
Classification Class II
Status Terminated
Quantity 4 vials
App-derived interpretation
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 for injectables and solutions intended to be sterile.
Code information Lot #: 02132019@25, Exp 5/14/19
Distribution pattern U.S.A. Nationwide
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[11382]
FDA event record
· Exact recall-number query on openFDA
drug · product 4 of 10
HCG (CHORIONIC GONADOTROPIN 1000 IU/ML PEP 25 mg/mL) inj 5 mL multidose vial compounded. Customceutical Compounding 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028 Ph. 480 516 0272
D-1256-2019
Recall number D-1256-2019
Initiated April 08, 2019
Classification Class II
Status Terminated
Quantity 12 vials
App-derived interpretation
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 for injectables and solutions intended to be sterile.
Code information Lot #: 03132019@23, Exp 5/12/19
Distribution pattern U.S.A. Nationwide
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[11126]
FDA event record
· Exact recall-number query on openFDA
drug · product 5 of 10
Lipoplex (METHIONINE 25 MG/ML INOSITOL 50 MG/ML CHOLINE CHLORIDE 50 MG/ML HYDROXOCOBALAMIN 500 MC/ML DEXPANTHENOL 50 MG/ML PYRIDOXINE HCL 50 MG/ML), 10 ML MULTIDOSE VIAL INJ COMPOUNDED. Customceutical Compounding 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028 Ph. 480 516 0272
D-1257-2019
Recall number D-1257-2019
Initiated April 08, 2019
Classification Class II
Status Terminated
Quantity 16 vials
App-derived interpretation
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 for injectables and solutions intended to be sterile.
Code information Lot #: 02212019@13, Exp 5/22/19
Distribution pattern U.S.A. Nationwide
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[11053]
FDA event record
· Exact recall-number query on openFDA
drug · product 6 of 10
Test D (TESTOSTERONE CYPIONATE 200MG/ML VITAMIN D3 5,000IU/ML), 5 ML MULTIDOSE VIAL COMPOUNDED. Customceutical Compounding 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028 Ph. 480 516 0272
D-1258-2019
Recall number D-1258-2019
Initiated April 08, 2019
Classification Class II
Status Terminated
Quantity 8 vials
App-derived interpretation
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 for injectables and solutions intended to be sterile.
Code information Lot #: 01232019@25, Exp 4/23/19
Distribution pattern U.S.A. Nationwide
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[10733]
FDA event record
· Exact recall-number query on openFDA
drug · product 7 of 10
Test D (TESTOSTERONE CYPIONATE 200MG/ML VITAMIN D3 5,000IU/ML), 5 ML MULTIDOSE VIAL COMPOUNDED. Customceutical Compounding 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028 Ph. 480 516 0272
D-1259-2019
Recall number D-1259-2019
Initiated April 08, 2019
Classification Class II
Status Terminated
Quantity 2 vials
App-derived interpretation
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 for injectables and solutions intended to be sterile.
Code information Lot #: 03132019@28, Exp 6/11/19
Distribution pattern U.S.A. Nationwide
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[10615]
FDA event record
· Exact recall-number query on openFDA
drug · product 8 of 10
Test PROCYP (TESTOSTERONE CYPIONATE 200MG/ML TESTOSTERONE PROPIONATE 20MG/ML), 5 ML MULTIDOSE VIAL INJ COMPOUNDED. Customceutical Compounding 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028 Ph. 480 516 0272
D-1260-2019
Recall number D-1260-2019
Initiated April 08, 2019
Classification Class II
Status Terminated
Quantity 5 vials
App-derived interpretation
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 for injectables and solutions intended to be sterile.
Code information Lot #: 03112019@10, Exp 6/19/19
Distribution pattern U.S.A. Nationwide
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[11326]
FDA event record
· Exact recall-number query on openFDA
drug · product 9 of 10
Trimix HIGH (Papaverine HCl 30 mg/mL Phentolamine Mesylate 2 mg/mL Alprostadil 20 mcg/mL), 2 mL multidose vial MDV Inj. Compounded. Customceutical Compounding 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028 Ph. 480 516 0272
D-1261-2019
Recall number D-1261-2019
Initiated April 08, 2019
Classification Class II
Status Terminated
Quantity 3 vials
App-derived interpretation
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 for injectables and solutions intended to be sterile.
Code information Lot #: 02182019@27, Exp 8/02/19
Distribution pattern U.S.A. Nationwide
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[10604]
FDA event record
· Exact recall-number query on openFDA
drug · product 10 of 10
TriMix MEDIUM (Papaverine HCL 21 mg/mL Phentolamine Mesylate 0.7 mg/mL Alprostadil 7 mcg/mL), 2 mL multidose MDV Inj. Compounded. Customceutical Compounding 4611 E. Shea Blvd. Bldg 3 180, Phoenix, AZ 85028 Ph. 480 516 0272
D-1262-2019
Recall number D-1262-2019
Initiated April 08, 2019
Classification Class II
Status Terminated
Quantity N/A
App-derived interpretation
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 for injectables and solutions intended to be sterile.
Code information Lot #: 02182019@22, Exp 8/02/19
Distribution pattern U.S.A. Nationwide
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[11330]
FDA event record
· Exact recall-number query on openFDA