HOSPIRA INC, LAKE FOREST FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

HOSPIRA INC, LAKE FOREST has 4 FDA recalls (1 Class I), 0 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "HOSPIRA INC, LAKE FOREST" is on file.

What these totals cover: FDA records filed under the name "HOSPIRA INC, LAKE FOREST". Records filed under related names are not included; see Related names.

Latest recall
D-0052-2027 · Sep 29, 2026 · filed under Pfizer
Latest recall under this name
D-0906-2018 · Class I · Jun 4, 2018

Newer recall under related name Pfizer: Sep 29, 2026, D-0052-2027.

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls4 (1 Class I)Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections0Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

HOSPIRA INC, LAKE FOREST's FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

HOSPIRA INC, LAKE FOREST: FDA recall records per year 2017: 3 recall records320172018: 1 recall records120182019: 0 recall records020192020: 0 recall records020202021: 0 recall records020212022: 0 recall records020222023: 0 recall records020232024: 0 recall records020242025: 0 recall records020252026: 0 recall records02026
YearInspectionsOAIWarning lettersRecall recordsClass I
202600000
202500000
202400000
202300000
202200000
202100000
202000000
201900000
201800011
201700030

Inspections are counted by the date they ended, warning letters by the date FDA issued them and recall records by the recall start date. FDA lists one recall record per recalled product, so one recall event can add several.

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Recent recalls

4 recall records from Jul 26, 2017 to Jun 4, 2018.

NumberClassProductDate
D-0906-2018Class INaloxone Hydrochloride Injection, USP, 0.4 mg/mL, 1 mL in 2.5 mL Carpuject Single-use cartridge…Jun 4, 2018
D-1080-2017Class IIHydromorphone Hydrochloride Injection, USP, 500 mg/50 mL (10 mg/mL), 50 mL Single Dose Vial. Mfd…Jul 26, 2017
D-1081-2017Class IIHydromorphone Hydrochloride Injection, USP, 500 mg/50 mL (10 mg/mL), 50 mL Single Dose Vial per…Jul 26, 2017
D-1082-2017Class IIHydromorphone Hydrochloride Injection, USP, 50 mg/5 mL (10 mg/mL), 5 mL Single Dose Vial.(10 vials…Jul 26, 2017

HOSPIRA INC, LAKE FOREST and the FDA: common questions

Has HOSPIRA INC, LAKE FOREST received an FDA warning letter?

No FDA warning letter addressed to the name "HOSPIRA INC, LAKE FOREST" is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has HOSPIRA INC, LAKE FOREST received an FDA Form 483?

FDA has not published a Form 483 for "HOSPIRA INC, LAKE FOREST" in its reading room. FDA publishes some Form 483s, not all of them.

Has HOSPIRA INC, LAKE FOREST had an FDA recall?

Yes. HOSPIRA INC, LAKE FOREST has 4 FDA recalls on record, 1 of them Class I, the most serious class. The most recent under this name started Jun 4, 2018. A newer recall, dated Sep 29, 2026, is filed under the related name Pfizer.

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Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.