Fresh Recalls

FDANot Yet Classified · Drug · FDA event 99388; recall number pending · Recalled July 29, 2026

Glycopyrrolate Oral Solution recall — Precision Dose Inc.

Agency report date: July 29, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Glycopyrrolate Oral Solution
Company / brand
Precision Dose
Lot / serial / date codes
Lot # 506033, Exp Date: 11/30/2026.
Distribution
US Nationwide.
Agency product description and boundaries

Glycopyrrolate Oral Solution, 1 mg/5 mL, delivers 5 mL, Rx only, Pkg: Precision Dose, Inc, S. Beloil, IL 61080, unit-dose oral syringes, NDCs 68094-073-01 (oral syringe) and 68094-073-58 (case).

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Due to an out-of-specification result for an unidentified impurity detected during routine stability testing.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Affected product: Glycopyrrolate Oral Solution

3. Open the official notice or contact

Official recall ID
Not yet assigned by the FDA — identified by FDA event ID 99388
Brand
Precision Dose
Classification
Not Yet Classified
Units affected
N/A
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
South Beloit, IL, United States
Firm address
722 Progressive Ln, N/A, 61080-2616

Identifying details (verbatim from the notice)

Product codes / lots
Lot # 506033, Exp Date: 11/30/2026.
Distribution
US Nationwide.
Firm notified the public via
Letter
FDA event ID
99388
Recall initiated
July 14, 2026
FDA report date
July 29, 2026
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved August 11, 2026 at 12:00 AM UTC.

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