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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 66172

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

Open FDA event record

Event summary

Timeline bucket
August 23, 2013
Product types
Drug
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Medaus, 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

Complete imported group

Every recalled product in this event

8 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 8

Testosterone Cyp 200 mg/mL, W/Pres. (Benzyl ETOH), 3 mL, Medaus pharmacy 1-800-526-9183

D-1048-2013
Recall number
D-1048-2013
Initiated
August 23, 2013
Classification
Class II
Status
Terminated
Recalling firm
Medaus, Inc.
Quantity
1198 mL

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
microbial 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: The product lots are being recalled due to laboratory results (from a contract lab) indicating microbial contamination. The FDA was concerned test results obtained from the recalling firm's contract testing lab may not be reliable. Hence the sterility of the products cannot be assured.

Code information

LOT # 130508-1, BUD: 11/16/2013

Distribution pattern

Nationwide

drug · product 2 of 8

Lipo-Injection w/ Lidocaine (PF), Ascorbic Acid 50 mg; B1-50 mg; B2-5-PO4-5 mg; B3-50 mg; B5-5 mg; B6-5 mg; Cyano B12-100 mcg; Methionine 12.5 mg; Inositol-25 mg; Choline-25 mg; Lidocaine 10 mg/mL, 30 mL, Medaus Pharmacy 1-800-526-9183

D-1049-2013
Recall number
D-1049-2013
Initiated
August 23, 2013
Classification
Class II
Status
Terminated
Recalling firm
Medaus, Inc.
Quantity
19,803 mL

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
microbial 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: The product lots are being recalled due to laboratory results (from a contract lab) indicating microbial contamination. The FDA was concerned test results obtained from the recalling firm's contract testing lab may not be reliable. Hence the sterility of the products cannot be assured.

Code information

Lot #: 130510-26, Exp 11/16/2013; 130610-24, Exp 12/7/2013; and 130709-68, Exp 1/5/2014

Distribution pattern

Nationwide

drug · product 3 of 8

Taurine 50 mg/mL PF, 100 mL, Medaus Pharmacy 1-800-526-9183

D-1050-2013
Recall number
D-1050-2013
Initiated
August 23, 2013
Classification
Class II
Status
Terminated
Recalling firm
Medaus, Inc.
Quantity
1660 mL

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
microbial 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: The product lots are being recalled due to laboratory results (from a contract lab) indicating microbial contamination. The FDA was concerned test results obtained from the recalling firm's contract testing lab may not be reliable. Hence the sterility of the products cannot be assured.

Code information

LOT # 130618-64, BUD: 12/15/2013

Distribution pattern

Nationwide

drug · product 4 of 8

L-Glutathione 200 mg/mL PF, 100 mL, Medaus Pharmacy 1-800-526-9183

D-1051-2013
Recall number
D-1051-2013
Initiated
August 23, 2013
Classification
Class II
Status
Terminated
Recalling firm
Medaus, Inc.
Quantity
6130 mL

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
microbial 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: The product lots are being recalled due to laboratory results (from a contract lab) indicating microbial contamination. The FDA was concerned test results obtained from the recalling firm's contract testing lab may not be reliable. Hence the sterility of the products cannot be assured.

Code information

LOT # 130617-10, Exp 12/14/2013

Distribution pattern

Nationwide

drug · product 5 of 8

Pyridoxine HCL 100 mg/mL NS (PF), 30 mL, Medaus Pharmacy 1-800-526-9183

D-1052-2013
Recall number
D-1052-2013
Initiated
August 23, 2013
Classification
Class II
Status
Terminated
Recalling firm
Medaus, Inc.
Quantity
2970 mL

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
microbial 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: The product lots are being recalled due to laboratory results (from a contract lab) indicating microbial contamination. The FDA was concerned test results obtained from the recalling firm's contract testing lab may not be reliable. Hence the sterility of the products cannot be assured.

Code information

LOT # 130531-31, Exp 11/27/2013

Distribution pattern

Nationwide

drug · product 6 of 8

Magnesium Chl 200 mg/mL PF, 100 mL, Medaus Pharmacy 1-800-526-9183

D-1053-2013
Recall number
D-1053-2013
Initiated
August 23, 2013
Classification
Class II
Status
Terminated
Recalling firm
Medaus, Inc.
Quantity
1880 mL

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
microbial 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: The product lots are being recalled due to laboratory results (from a contract lab) indicating microbial contamination. The FDA was concerned test results obtained from the recalling firm's contract testing lab may not be reliable. Hence the sterility of the products cannot be assured.

Code information

LOT # 130307-60, Exp 9/3/2013

Distribution pattern

Nationwide

drug · product 7 of 8

NA Ascorbate 500 mg/mL, PF, 100 mL, Medaus Pharmacy 1-800-526-9183

D-1054-2013
Recall number
D-1054-2013
Initiated
August 23, 2013
Classification
Class II
Status
Terminated
Recalling firm
Medaus, Inc.
Quantity
15,500 mL

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
microbial 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: The product lots are being recalled due to laboratory results (from a contract lab) indicating microbial contamination. The FDA was concerned test results obtained from the recalling firm's contract testing lab may not be reliable. Hence the sterility of the products cannot be assured.

Code information

LOT # 130702-1, Exp 12/29/2013

Distribution pattern

Nationwide

drug · product 8 of 8

NA Ascorbate 500 mg/mL, non corn PF, 100ML, Medaus Pharmacy, 1-800-526-9183

D-1055-2013
Recall number
D-1055-2013
Initiated
August 23, 2013
Classification
Class II
Status
Terminated
Recalling firm
Medaus, Inc.
Quantity
8750 mL

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
microbial 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: The product lots are being recalled due to laboratory results (from a contract lab) indicating microbial contamination. The FDA was concerned test results obtained from the recalling firm's contract testing lab may not be reliable. Hence the sterility of the products cannot be assured.

Code information

LOT # 130613-8, Exp 12/10/2013

Distribution pattern

Nationwide