Cinacalcet Hydrochloride Tablets, 30 mg recall — Cipla Usa, Inc. (Class II)

Cipla Usa, Inc. is recorded by the U.S. Food and Drug Administration (FDA) as recalling Cinacalcet Hydrochloride Tablets, 30 mg — a Class II recall, initiated 2026-06-29 and posted to the FDA enforcement report on 2026-07-08, under recall number D-0661-2026. Status Ongoing, with no termination date on the record. The reason the FDA record carries is, verbatim: “cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI).”. From the product description, the form is tablets, the strength given is 30 mg, the package is described as 30-count bottle and it is marked Rx only. 1 National Drug Code number is printed in the record: 69097-410-02. Distribution is recorded as “USA Nationwide” — Nationwide (US), with the recalling firm on record in NJ, United States. The FDA files it under event ID 99350 together with 2 other recall numbers, all listed and linked below. Within that event this is the strength 30 mg and ndc 69097-410-02 configuration; the sibling records differ on strength and ndc and match on everything else the source states. Values are reproduced from the linked openFDA report; regulatory information, not medical advice.

Regulatory snapshot

Recall number D-0661-2026
FDA event ID 99350 (3 recall numbers)
Classification Class II (intermediate regulatory tier)
Status Ongoing
Recalling firm Cipla Usa, Inc.
Recall initiated 2026-06-29
Reported by FDA 2026-07-08
Report lag 9 days from initiation to report
Distribution USA Nationwide — Nationwide (US)
Firm location on record NJ, United States
Product description (source) Cinacalcet Hydrochloride Tablets, 30 mg, 30-count bottle, Rx Only, Manufactured by: Cipla Ltd., MIDC, Patalganga, India; Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059, NDC 69097-410-02

Reason reported by FDA

cGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI).

11 words from the enforcement report field reason_for_recall, reproduced without edit — the firm's own wording, not an assessment.

Product identifiers in this record

7 identifying values matched by exact pattern in the 31-word product description above; each is a literal substring of it.

Product named Cinacalcet Hydrochloride Tablets
Form Tablets
Strength 30 mg
Package 30-count bottle
NDC 69097-410-02
Marketing category Rx only
Manufactured by Cipla Ltd., MIDC
Manufactured for Cipla USA, Inc.

Which configuration this record is

3 recall numbers share event 99350. They differ on strength and ndc and agree on everything else the source states, so those are the values to check a package against.

Attribute This record (D-0661-2026) D-0675-2026D-0676-2026
Strength 30 mg 60 mg90 mg
NDC 69097-410-02 69097-411-0269097-412-02

Shared across all 3 records under this event: package 30-count bottle; form Tablets; product named Cinacalcet Hydrochloride Tablets; fda tier Class II; recalling firm Cipla Usa, Inc.; the same reason text; initiated 2026-06-29; reported 2026-07-08.

Event context: 3 recall numbers under event 99350

One enforcement action, 3 recall numbers: the FDA filed 2 further configurations of this action under event 99350. Each keeps its own recall number and dates.

Recall recordRecall numberFDA tierStrength / formNDCReported
Cinacalcet Hydrochloride Tablets, 60 mgD-0675-2026Class II60 mg · Tablets69097-411-022026-07-08
Cinacalcet Hydrochloride Tablets, 90 mgD-0676-2026Class II90 mg · Tablets69097-412-022026-07-08

Reported in the same month (2026-07)

111 enforcement reports carry a report date in 2026-07; these 8 are the Class II ones nearest this record.

Recall recordRecall numberRecalling firmFDA tierReported
BD ChloraPrep Hi-Lite Orange, 2%D-0643-2026Carefusion 213, LLCClass II2026-07-08
BD PurPrep, 8.3%D-0644-2026Carefusion 213, LLCClass II2026-07-08
BD ChloraPrep Clear, 2%D-0645-2026Carefusion 213, LLCClass II2026-07-08
ChloraPrep FREPP, 2%D-0646-2026Carefusion 213, LLCClass II2026-07-08
BD ChloraPrep Hi-Lite Orange, 2%D-0647-2026Carefusion 213, LLCClass II2026-07-08
BD ChloraPrep Hi-Lite Orange, 2%D-0648-2026Carefusion 213, LLCClass II2026-07-08
BD ChloraPrep Scrub Teal, 2%D-0649-2026Carefusion 213, LLCClass II2026-07-08
BD ChloraPrep Scrub Teal, 2%D-0650-2026Carefusion 213, LLCClass II2026-07-08

Nearest Class II recalls by date

213 of 250 indexed records share the Class II tier; the 6 nearest to 2026-07-08 by report date are listed here.

Recall recordRecall numberRecalling firmStrength / formReported
BD ChloraPrep CLear, 2%D-0651-2026Carefusion 213, LLC2% · Solution2026-07-08
BD ChloraPrep CLear, 2%D-0652-2026Carefusion 213, LLC2% · Solution2026-07-08
IMULDOSA, 130 mg/26 mLD-0653-2026Accord Biopharma Inc130 mg/26 mL · Injection2026-07-08
prednisoLONE Acetate Ophthalmic Suspension, 1%D-0655-2026Lupin Pharmaceuticals Inc.1% · Ophthalmic Suspension2026-07-08
Levothyroxine Sodium Tablets, 300 mcgD-0656-2026Accord Healthcare, Inc.300 mcg · Tablets2026-07-08
Synjardy XR Tablets, 1000 mgD-0657-2026Boehringer Ingelheim Pharmaceuticals, Inc.1000 mg · Extended-Release Tablets2026-07-08

Reading this record

Class II is the FDA's own severity tier for the recall action — 213 of the 250 indexed records carry it — and it describes the agency's assessment of the action, not a risk statement about any individual. A search on event 99350 returns all 3 of these recall numbers; a search on D-0661-2026 returns only this configuration. Match a package against 69097-410-02 at the FDA source to confirm it is covered.

Namespace context: the Class II index (213 records) and the recall hub (250 records, 118 FDA events); Cipla Usa, Inc. (3 indexed records) aggregates this firm across datasets.

Coverage and limits of this record

This page reflects the openFDA enforcement report for D-0661-2026 as ingested on 2026-08-22, which can lag the live FDA record and omits detail held only in primary documents. It offers no clinical assessment, no advice about whether to use any product, and no substitute. For any health question consult a qualified healthcare professional.

Source & provenance

Official source
https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0661-2026%22
Source dataset
openFDA Drug Enforcement API
Publication date
2026-07-08
Ingested
2026-08-22
Record hash
40f8d00e70f4b748

Verify every value against the official FDA source above. This site links to the regulator's record rather than replacing it.