Recall events
/
Event 78828
Event summary
Timeline bucket December 27, 2017
Product types Drug
Classifications Class II
Statuses Terminated
Recalling firm wording Pharmedium Services, LLC
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
42 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 42
HYDROmorphone HCl in Sodium Chloride 0.9% in all doses, all strengths, and all packaging.
D-0428-2018
Recall number D-0428-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9561]
FDA event record
· Exact recall-number query on openFDA
drug · product 2 of 42
Bupivacaine HCl in 0.9% Sodium Chloride in all doses, all strengths, and packaging.
D-0429-2018
Recall number D-0429-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity 297 bags
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9564]
FDA event record
· Exact recall-number query on openFDA
drug · product 3 of 42
Fentanyl Citrate and Ropivacaine HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
D-0430-2018
Recall number D-0430-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9742]
FDA event record
· Exact recall-number query on openFDA
drug · product 4 of 42
Fentanyl Citrate and Bupivacaine HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
D-0431-2018
Recall number D-0431-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9563]
FDA event record
· Exact recall-number query on openFDA
drug · product 5 of 42
Ephedrine Sulfate in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
D-0432-2018
Recall number D-0432-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9745]
FDA event record
· Exact recall-number query on openFDA
drug · product 6 of 42
HYDROmorphone HCl Injection in all strengths, all doses, and all packaging.
D-0433-2018
Recall number D-0433-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9856]
FDA event record
· Exact recall-number query on openFDA
drug · product 7 of 42
Midazolam HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
D-0434-2018
Recall number D-0434-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[10170]
FDA event record
· Exact recall-number query on openFDA
drug · product 8 of 42
Midazolam HCl in 5% Dextrose in all strengths, all doses, and all packaging.
D-0435-2018
Recall number D-0435-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9586]
FDA event record
· Exact recall-number query on openFDA
drug · product 9 of 42
Morphine Sulfate in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
D-0436-2018
Recall number D-0436-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9851]
FDA event record
· Exact recall-number query on openFDA
drug · product 10 of 42
Morphine Sulfate in 5% Dextrose in all strengths, all doses, and all packaging.
D-0437-2018
Recall number D-0437-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9737]
FDA event record
· Exact recall-number query on openFDA
drug · product 11 of 42
Lidocaine HCl in all strengths, all doses, and all packaging.
D-0438-2018
Recall number D-0438-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9970]
FDA event record
· Exact recall-number query on openFDA
drug · product 12 of 42
Fentanyl Citrate in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
D-0439-2018
Recall number D-0439-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9947]
FDA event record
· Exact recall-number query on openFDA
drug · product 13 of 42
Potassium Chloride in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
D-0440-2018
Recall number D-0440-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9845]
FDA event record
· Exact recall-number query on openFDA
drug · product 14 of 42
Ketamine HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
D-0441-2018
Recall number D-0441-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9740]
FDA event record
· Exact recall-number query on openFDA
drug · product 15 of 42
Succinylcholine Chloride in all strengths, all doses, and all packaging.
D-0442-2018
Recall number D-0442-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9577]
FDA event record
· Exact recall-number query on openFDA
drug · product 16 of 42
Adenosine Injection in all strengths, all doses, and all packaging.
D-0443-2018
Recall number D-0443-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9584]
FDA event record
· Exact recall-number query on openFDA
drug · product 17 of 42
Dexamethasone Sodium Phosphate in all strengths, all doses, and all packaging.
D-0444-2018
Recall number D-0444-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9612]
FDA event record
· Exact recall-number query on openFDA
drug · product 18 of 42
Phenylephrine HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
D-0445-2018
Recall number D-0445-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9957]
FDA event record
· Exact recall-number query on openFDA
drug · product 19 of 42
Potassium Chloride in 5% Dextrose in all strengths, all doses, and all packaging.
D-0446-2018
Recall number D-0446-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9921]
FDA event record
· Exact recall-number query on openFDA
drug · product 20 of 42
Labetalol HCl in all strengths, all doses, and all packaging.
D-0447-2018
Recall number D-0447-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9558]
FDA event record
· Exact recall-number query on openFDA
drug · product 21 of 42
Methadone HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
D-0448-2018
Recall number D-0448-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9923]
FDA event record
· Exact recall-number query on openFDA
drug · product 22 of 42
Midazolam HCl Injection in all strengths, all doses, and all packaging.
D-0449-2018
Recall number D-0449-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9756]
FDA event record
· Exact recall-number query on openFDA
drug · product 23 of 42
Fentanyl Citrate Injection in all strengths, all doses, and all packaging.
D-0450-2018
Recall number D-0450-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9903]
FDA event record
· Exact recall-number query on openFDA
drug · product 24 of 42
Ephedrine Sulfate Injection in all strengths, all doses, and all packaging.
D-0451-2018
Recall number D-0451-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9541]
FDA event record
· Exact recall-number query on openFDA
drug · product 25 of 42
Ketamine HCl Injection in all strengths, all doses, and all packaging.
D-0452-2018
Recall number D-0452-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9862]
FDA event record
· Exact recall-number query on openFDA
drug · product 26 of 42
Ropivacaine HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
D-0453-2018
Recall number D-0453-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9946]
FDA event record
· Exact recall-number query on openFDA
drug · product 27 of 42
Glycopyrrolate in all strengths, all doses, and all packaging.
D-0454-2018
Recall number D-0454-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9557]
FDA event record
· Exact recall-number query on openFDA
drug · product 28 of 42
Lidocaine HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
D-0455-2018
Recall number D-0455-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9595]
FDA event record
· Exact recall-number query on openFDA
drug · product 29 of 42
Atropine Sulfate Injection in all strengths, all doses, and all packaging.
D-0456-2018
Recall number D-0456-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9930]
FDA event record
· Exact recall-number query on openFDA
drug · product 30 of 42
HYDROmorphone HCl in 5% Dextrose in all strengths, all doses, and all packaging.
D-0457-2018
Recall number D-0457-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9958]
FDA event record
· Exact recall-number query on openFDA
drug · product 31 of 42
Ropivacaine HCl Injection in all strengths, all doses, and all packaging.
D-0458-2018
Recall number D-0458-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[10175]
FDA event record
· Exact recall-number query on openFDA
drug · product 32 of 42
Nicardipine HCl in all strengths, all doses, and all packaging.
D-0459-2018
Recall number D-0459-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9975]
FDA event record
· Exact recall-number query on openFDA
drug · product 33 of 42
Labetalol HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
D-0460-2018
Recall number D-0460-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[7203]
FDA event record
· Exact recall-number query on openFDA
drug · product 34 of 42
Neostigmine Methylsulfate Injection in all strengths, all doses, and all packaging.
D-0461-2018
Recall number D-0461-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9607]
FDA event record
· Exact recall-number query on openFDA
drug · product 35 of 42
Vecuronium Bromide in Sterile Water for Injection in all strengths, all doses, and all packaging.
D-0462-2018
Recall number D-0462-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9963]
FDA event record
· Exact recall-number query on openFDA
drug · product 36 of 42
Dexamethasone Sodium Phosphate added to 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
D-0463-2018
Recall number D-0463-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[10149]
FDA event record
· Exact recall-number query on openFDA
drug · product 37 of 42
Esmolol HCl in all strengths, all doses, and all packaging.
D-0464-2018
Recall number D-0464-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9553]
FDA event record
· Exact recall-number query on openFDA
drug · product 38 of 42
Meperidine HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
D-0465-2018
Recall number D-0465-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9868]
FDA event record
· Exact recall-number query on openFDA
drug · product 39 of 42
Methadone HCl Injection in all strengths, all doses, and all packaging.
D-0466-2018
Recall number D-0466-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[7668]
FDA event record
· Exact recall-number query on openFDA
drug · product 40 of 42
Rocuronium Bromide in all strengths, all doses, and all packaging.
D-0467-2018
Recall number D-0467-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9926]
FDA event record
· Exact recall-number query on openFDA
drug · product 41 of 42
Dexamethasone Sodium Phosphate added to 5% Dextrose in all strengths, all doses, and all packaging.
D-0468-2018
Recall number D-0468-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9614]
FDA event record
· Exact recall-number query on openFDA
drug · product 42 of 42
Nicardipine HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
D-0469-2018
Recall number D-0469-2018
Initiated December 27, 2017
Classification Class II
Status Terminated
Quantity Unknown
App-derived interpretation
Sterility assurance
reason.sterility_assurance · v1.0.0
Lack of sterility
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Lack of sterility assurance.
Code information All lots remaining within expiry.
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[9918]
FDA event record
· Exact recall-number query on openFDA
