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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 81413

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

Open FDA event record

Event summary

Timeline bucket
October 19, 2018
Product types
Drug
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Avella of Deer Valley, Inc. Store 38

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

5 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 5

Morphine (1 mg/mL) in NS 100 mL Bag, Rx only, Advanced Pharma, Inc. d/b/a Avella of Houston, and Avella of Deer Valley, Inc. #38

D-0131-2019
Recall number
D-0131-2019
Initiated
October 19, 2018
Classification
Class II
Status
Terminated
Quantity
1,360 bags

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

Code information

Lot # 7/10/18 0415 24110P, Exp 11/07/2018; 7/25/18 0247 24110P, Exp 11/22/2018

Distribution pattern

U.S.A. nationwide.

drug · product 2 of 5

Fentanyl (10 mcg/mL) in NS 1 mL (in 3mL BD Syringe), Rx only, Advanced Pharma, Inc. d/b/a Avella of Houston, and Avella of Deer Valley, Inc. #38

D-0132-2019
Recall number
D-0132-2019
Initiated
October 19, 2018
Classification
Class II
Status
Terminated
Quantity
20 syringes

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

Code information

Lot # 8/8/18 0200 15-21070S, Exp 11/06/2018

Distribution pattern

U.S.A. nationwide.

drug · product 3 of 5

Hydromorphone (0.2 mg/mL) in NS 100 mL Bag, Rx only, Advanced Pharma, Inc. d/b/a Avella of Houston, and Avella of Deer Valley, Inc. #38

D-0133-2019
Recall number
D-0133-2019
Initiated
October 19, 2018
Classification
Class II
Status
Terminated
Quantity
360 bags

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

Code information

Lot # 8/27/18 0215 22110P, Exp 12/10/2018

Distribution pattern

U.S.A. nationwide.

drug · product 4 of 5

Phenylephrine 25 mg added to NS 250 mL Bag, Rx only, Advanced Pharma, Inc. d/b/a Avella of Houston, and Avella of Deer Valley, Inc. #38

D-0134-2019
Recall number
D-0134-2019
Initiated
October 19, 2018
Classification
Class II
Status
Terminated
Quantity
300 bags

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

Code information

Lot# 138-20182308@88, Exp 11/06/2018

Distribution pattern

U.S.A. nationwide.

drug · product 5 of 5

Phenylephrine 30 mg added to NS 250 mL Bag, Rx only, Advanced Pharma, Inc. d/b/a Avella of Houston, and Avella of Deer Valley, Inc. #38

D-0135-2019
Recall number
D-0135-2019
Initiated
October 19, 2018
Classification
Class II
Status
Terminated
Quantity
300 bags

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

Code information

Lot# 138-20180409@55, Exp 11/18/2018

Distribution pattern

U.S.A. nationwide.

Field note

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