Hazard

Cgmp Non Compliance recalls

9 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total: 9
Critical: 0
Severe: 0
Most recent: 2022-02-09

Of the 9 cgmp non compliance recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.

Which agencies issued them

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all cgmp non compliance recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

1–9 of 9

ModerateFDA (Drugs)·D-0497-2022·2022-02-09
Pain & Sinus Reliever tablets recalled for manufacturing deviations
Ultra Seal Corporation is recalling 887,000 packets of Pain & Sinus Reliever (acetaminophen/phenylephrine) tablets nationwide due to cGMP manufacturing deviations. The recalled product is identified by Lot #AK9527 with expiration date 03/2022.
Product
Pain & Sinus Reliever Pain Reliever/Nasal Decongestant (acetaminophen 500mg, Phenylephrine HCl 5mg) 2 tablet packets, Mfg for Advanced First Aid, Baltimore, MD 21237, NDC 67060-194-68
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0438-2022·2022-02-02
Lidocaine HCl / Oxymetazoline HCl Nasal Solution Recalled for CGMP Deviations
Edge Pharma, LLC is recalling Lidocaine HCl / Oxymetazoline HCl Nasal Solution (4% / 0.05%, 240mL) nationwide due to Current Good Manufacturing Practice (CGMP) deviations.
Product
Lidocaine HCl / Oxymetazoline HCl Nasal Solution, 4% / 0.05%, 240mL per bottle, Multiple Dose Container for Intranasal Use, Edge Pharma, LLC, 856 Hercules Dr., Colchester, VT 05446, NDC 05446-1256-01, packaged in bottles. no label
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0839-2021·2021-10-06
Neutrogena Ultra Sheer Sunscreen Recalled for cGMP Deviations
Johnson & Johnson Consumer is voluntarily recalling Neutrogena Ultra Sheer body mist sunscreen SPF 100+ nationwide due to manufacturing deviations. Approximately 3.98 million cans are affected.
Product
Neutrogena Ultra Sheer body mist sunscreen BROAD SPECTRUM SPF 100+, Avobenzone (3%), Homosalate (15%), Octisalate (5%), Octocrylene (10%), Oxybenzone (15%), NET WT. 5.0 OZ (141 g) aerosol can, Distributed by: JOHNSON & JOHNSON CONSUMER INC. Skillman, NJ 08858, UPC 0 86800 10041 6
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0840-2021·2021-10-06
Neutrogena COOLDRY SPORT Sunscreen Spray Recalled Due to cGMP Deviations
Johnson & Johnson Consumer, Inc. is recalling 405,264 cans of Neutrogena COOLDRY SPORT Broad Spectrum SPF 100 sunscreen spray nationwide due to current good manufacturing practice (cGMP) deviations. This is a voluntary recall initiated by the firm.
Product
Neutrogena COOLDRY SPORT sunscreen spray BROAD SPECTRUM SPF 100, Avobenzone (3%), Homosalate (15%), Octisalate (5%), Octocrylene (10%), Oxybenzone (6%) aerosol can, NET WT. 5.0 OZ (141 g) Distributed by: JOHNSON & JOHNSON CONSUMER, INC. Skillman, NJ 08858, UPC 0 86800 10143 7
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0180-2020·2019-11-27
Basic Reset Recalls Body Mass Reset for CGMP Non-Compliance
Basic Reset Inc. is recalling Body Mass Reset dietary supplements because they do not conform to Dietary Supplement CGMP regulations.
Product
Body Mass Reset, 4 fl. oz. plastic bottle, SKU: 100-8C
Category
Food
Distribution
0 states
ModerateFDA (Food)·F-0182-2020·2019-11-27
Basic Reset Recalls Q-min Dietary Supplement for CGMP Non-Compliance
Basic Reset Inc. is recalling Q-min dietary supplements because they do not conform to Dietary Supplement CGMP regulations. The product was distributed to all 50 states and several foreign countries.
Product
Q-min, 50 capsules per plastic bottle, SKU: 100-9B
Category
Food
Distribution
0 states
ModerateFDA (Food)·F-0177-2020·2019-11-27
Basic Reset pH-FX Dietary Supplement Recalled for CGMP Non-Compliance
Basic Reset Inc. is recalling pH-FX dietary supplements because they do not conform to Dietary Supplement CGMP regulations. The product was distributed to all 50 states and several foreign countries.
Product
pH-FX 4 fl. oz. plastic bottle, SKU: 100-1A
Category
Food
Distribution
0 states
ModerateFDA (Food)·F-1239-2020·2019-11-27
Basic Reset Dino Min Dietary Supplement Recalled for CGMP Non-Compliance
Basic Reset Inc. is recalling Dino Min dietary supplements because they do not conform to Dietary Supplement CGMP regulations. The product was distributed to all 50 states and several foreign countries.
Product
Dino Min, 60 capsules per plastic bottle, SKU: 100-1C
Category
Food
Distribution
0 states
ModerateFDA (Food)·F-0178-2020·2019-11-27
Basic Reset Recalls SlimUp Dietary Supplement for CGMP Non-Compliance
Basic Reset Inc. is recalling SlimUp dietary supplements because they do not conform to Dietary Supplement CGMP regulations. The product was distributed to all 50 states and several foreign countries.
Product
SlimUp 60 capsules per plastic bottle, SKU: 100-5B
Category
Food
Distribution
0 states