Safecor Health Recalls Calcium Carbonate Tablets Due to CGMP Deviations
Safecor Health, LLC is recalling Calcium Carbonate 600mg/Vitamin D3 tablets due to Current Good Manufacturing Practice (CGMP) deviations. Check your lot number.
Recall notice
CGMP Deviations
Contact the company
What happened, in plain English
Safecor Health, LLC has recalled one lot of Calcium Carbonate 600mg/Vitamin D3 400 International Units tablets because of Current Good Manufacturing Practice (CGMP) deviations. The recall affects 25 bottles distributed in Massachusetts and New York. The specific nature of the deviation is not detailed in the record. Read more at govinfonow.com/recall/42552-safecor-health-recalls-calcium-carbonate-tablets-due-to-cgmp-deviations.
Source Summary by GovInfoNow · govinfonow.com/recall/42552-safecor-health-recalls-calcium-carbonate-tablets-due-to-cgmp-deviations · Updated October 9, 2026 · FDA enforcement record: FDA #D-0902-2017
Cite this page
“Safecor Health Recalls Calcium Carbonate Tablets Due to CGMP Deviations.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/42552-safecor-health-recalls-calcium-carbonate-tablets-due-to-cgmp-deviations. Based on FDA recall #D-0902-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0902-2017%22&limit=1).
Why it’s dangerous
The recall is due to deviations from Current Good Manufacturing Practice (CGMP) standards. The record does not specify what these deviations were or how they might affect the safety or efficacy of the tablets.
Who’s affected
Consumers who purchased Calcium Carbonate tablets from Safecor Health in Massachusetts or New York before July 7, 2016. Individuals taking this specific supplement are at risk if their product matches the recalled lot.
How to tell if you have this one
Check your bottle for the brand 'Safecor Health', NDC 00904323392, and Lot # A18705. The expiration date on the bottle should be 09/30/2017. The product contains 60 tablets per bottle.
- Brand
Safecor Health- Category
Drug
All 6 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
MA and NY
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-0900-2017 | Acetaminophen 325mg tablets, 120-count bottles, Pk By Safecor Health Woburn, MA 01801, NDC 00904198280.; Lot #: A18688, Exp. 09/30/2018 | 66 bottles |
| D-0901-2017 | Atorvastatin Calcium 40mg Tablet, 30-count bottles, Rx only, Pk By Safecor Health Woburn, MA 01801, NDC 60505258009; Lot # A18661, Exp. 10/31/2017 | 119 bottles |
| D-0902-2017 | Calcium Carbonate 600mg/Vitamin D3 400 International Units tablets, 60-count bottles, Pk By Safecor Health Woburn, MA 01801, NDC 00904323392.; Lot # A18705, Exp. 09/30/2017 | 25 bottles |
| D-0903-2017 | Acyclovir 400mg Tablet, 15-count bottles, Rx only, Packaged by Safecor Health, LLC. Woburn, MA 01801, NDC 0093894305; Lot # A25591, Exp. 02/22/2017 | 601 bottles |
| D-0904-2017 | Doxycycline100mg Tablets, 14-count bottles, Rx only, Packaged By Safecor Health LLC Woburn, MA 01801, NDC 0143314205; Lot # A25593, Exp. 2/22/2017 | 856 bottles |
| D-0905-2017 | Metronidazole 500mg Tablet, 50-count bottles, Rx only, Packaged By Safecor Health LLC Woburn, MA 01801, NDC 5011133402; Lot # A25593, Exp. 02/22/2017 | 1,933 bottles |
Where it went and when
Where it was distributed
Distributed in Massachusetts and New York.
FDA distribution: “MA and NY” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Massachusetts, New York.
Recall timeline
FDA terminated this recall 12 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-0902-2017 (July 7, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0902-2017 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 9, 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.