Drug recall

70% Human Insulin Isophane Suspension 30% Human Insulin Injection (rDNA origin), U-100, 100 units/mL human…

FDA recall event 29910 · Class III · Walgreen Company

Key facts

Event ID 29910
Recall numbers D-001-5, D-002-5, D-003-5, D-004-5, D-005-5, D-006-5, D-007-5, D-008-5, D-009-5, D-010-5, D-011-5, D-012-5 and 13 more
Recalling firm Walgreen Company
Product type Drugs
Products 70% Human Insulin Isophane Suspension 30% Human Insulin Injection (rDNA origin), U-100, 100 units/mL human insulin, OTC, distributed under the following labels and containers: a) Humulin 70/30…, Bausch & Lomb Desmopressin Acetate Nasal Solution, 0.01%, 5 mL bottle with spray attachment, delivering 0.1 mL per actuation, Rx antidiuretic hormone, Bausch & Lomb Inc., Tampa, FL 33637, NDC…, CombiPatch 50/140 Transdermal Patch, estradiol/norethindrone acetate transdermal system, 0.05/0.14 mg per day, Rx contraceptive patch, 8 patches per box, 3 boxes per case, Manufactured by Noven…, CombiPatch 50/250 Transdermal Patch, estradiol/norethindrone acetate transdermal system, 0.05/0.25 mg per day, Rx contraceptive patch, 8 patches per box, 3 boxes per case, Manufactured by Noven…, Erythromycin Ethylsuccinate Oral Suspension, USP, 200 mg/5 mL , one pint bottle, Rx, Abbott Laboratories, North Chicago, IL 60064, NDC 0074-3747-16, Walgreen item 677076 and 20 more
Classification Class III
Status Ongoing
Voluntary or mandated Firm Initiated
Reason for recall Inadvertent distribution of refrigerated drugs which had been subject to a two day power outage resulting from hurricane Charley.
Initiation date Aug 17, 2004
City Deerfield
Country United States
FEI number 1460851

At a glance

  • 10–99 Products in this recall
  • 1–9 FDA inspections of this firm (FEI)

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. Food and Drug Administration (FDA), Enforcement Reports

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