Longbow Emergency Eyewash Recall: CGMP Deviations in Purified Water
Longbow recalls emergency eyewash bottles with CGMP deviations. These purified water products may have quality issues affecting safety. Consumers should check product labels for NDC 7110500002 or 71150000.
Recall notice
CGMP Deviations
Contact the company
What happened, in plain English
Longbow recalls emergency eyewash bottles that contain purified water (98.3% purity) due to manufacturing quality control issues. This recall affects products sold with specific National Drug Codes (NDCs) that may not meet safety standards. Read more at govinfonow.com/recall/40354-longbow-emergency-eyewash-recall-cgmp-deviations-in-purified-water.
Source Summary by GovInfoNow · govinfonow.com/recall/40354-longbow-emergency-eyewash-recall-cgmp-deviations-in-purified-water · Updated October 6, 2026 · FDA enforcement record: FDA #D-1048-2018
Cite this page
“Longbow Emergency Eyewash Recall: CGMP Deviations in Purified Water.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/40354-longbow-emergency-eyewash-recall-cgmp-deviations-in-purified-water. Based on FDA recall #D-1048-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1048-2018%22&limit=1).
Why it’s dangerous
The recall is due to CGMP (Current Good Manufacturing Practice) deviations, which means the product was made without following proper quality control standards. This could lead to the eyewash not being safe or effective for emergency use.
Who’s affected
People who own or use the recalled emergency eyewash bottles with NDC numbers 7110500002 or 71150000 are affected. Those who use these products for eye irrigation in emergencies are at risk due to potential quality issues.
How to tell if you have this one
Check for the product name 'Emergency First Aid Eyewash (Purified Water 98.3%)' on the bottle. Look for NDC numbers 7110500002 (4 fl oz) or 71150000 (0.67 fl oz).
- Brand
Longbow First Aid Products- Category
Drug
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
NY and CA.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-1048-2018 | Emergency First Aid Eyewash (Purified Water 98.3%), packaged in a) 4fl oz. (118 ml) NDC 7110500002, and b) 0.67 fl (20 ml) NDC 71150000) bottles, Manufactured for: Redicare LLC, Congers, NY; Lot #: a) 20171210, Exp. 12/2022; b) 20171210, Exp. 12/2022 | 30,000 bottles |
| D-1049-2018 | Eyewash Purified water 98.3%, Ophthalmic Solution, packaged in a) 4 FL OZ (NDC 6910-3218-07) and b) 8 Fl OZ (NDC 6910-3218-08) bottles, 77656 Flora Rd, Palm Desert, CA 92211.; Lot #: a) 20171215 and 20171016, b) 20171016 | 14,400 bottles |
What to do — step by step
Check Product Labels
Look for NDC numbers 7110500002 or 71150000 on the bottle to confirm if it's recalled.
Where it went and when
Where it was distributed
Distributed in California and New York.
FDA distribution: “NY and CA.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, New York.
Recall timeline
FDA terminated this recall 14 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-1048-2018 (July 17, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1048-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 6, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.