Recall Register

Food, drugs, devices

Food recall: Bio Armor Carno Pump Plus Electrolytes 40 servings (Blue Raspberry), Distributed by Reaction Nutrition, Carnegie, PA

FDA enforcement event 71095 · Class II · initiated 15 Apr 2015 · status Terminated · terminated 21 Nov 2018

FoodVoluntary: Firm initiated13 product recordsCarnegie, PA

FDA enforcement event 71095 is a food recall by Reaction Nutrition LLC of Carnegie, PA, initiated 15 Apr 2015 and classified Class II, with 13 product records.

FDA defines Class II as a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. 46% of the 607 food enforcement events initiated in 2015 carry the same class.

Status: Terminated, terminated 21 Nov 2018. Initiation: voluntary: firm initiated. Reaction Nutrition LLC has 2 enforcement events on this register, with a median of 13 product records per event.

Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.

Recalling firm

Reaction Nutrition LLC, Carnegie, PA.

Reason for recall

"Work out support nutritional supplements manufactured on shared equipment may contain unknown amounts of whey protein and soy."

Distribution

"nationwide to retailers and consumers"

Product records

Recall numberProductQuantityClassStatusReport date
F-2389-2015Bio Armor Carno Pump Plus Electrolytes 40 servings (Blue Raspberry), Distributed by Reaction Nutrition, Carnegie, PA600Class IITerminated17 Jun 2015
F-2390-2015Bio Armor Carno Pump Plus Electrolytes 40 servings (Cherry Lime), Distributed by Reaction Nutrition, Carnegie, PA564Class IITerminated17 Jun 2015
F-2391-2015Bio Armor CreaMatrix 306g 60 servings Unflavored, Distributed by Reaction Nutrition, Carnegie, PA834Class IITerminated17 Jun 2015
F-2392-2015Bio Armor CreaMatrix 60 servings Blue Raspberry, Distributed by Reaction Nutrition, Carnegie, PA594Class IITerminated17 Jun 2015
F-2393-2015Bio Armor CreaMatrix 60 servings Cherry Lime, Distributed by Reaction Nutrition, Carnegie, PA896Class IITerminated17 Jun 2015
F-2394-2015Bio Armor Glutamine 150 Grams and Bio Armor Glutamine 500 Grams, Distributed by Reaction Nutrition, Carnegie, PA1,105Class IITerminated17 Jun 2015
F-2395-2015REACTION RECOR: Amino Action- 500g (Cherry Lime), Distributed by Reaction Nutrition, Carnegie, PA1,302Class IITerminated17 Jun 2015
F-2396-2015REACTION RECOR: Amino Action- 500g (Glacier Blue), Distributed by Reaction Nutrition, Carnegie, PA1,108Class IITerminated17 Jun 2015
F-2397-2015RN BlueChip: Glutamine, L-Glutamine Powder, 400 grams, Distributed by Reaction Nutrition, Carnegie, PA366Class IITerminated17 Jun 2015
F-2398-2015RN BlueChip: Creatine, Creatine Monohydrate, 400 grams, Distributed by Reaction Nutrition, Carnegie, PA529Class IITerminated17 Jun 2015
F-2399-2015REACTION RECOR: Pre Action- 336g Orange Xplosion, Distributed by Reaction Nutrition, Carnegie, PA926Class IITerminated17 Jun 2015
F-2400-2015REACTION RECOR: Pre Action- 336g Glacier Blue, Distributed by Reaction Nutrition, Carnegie, PA823Class IITerminated17 Jun 2015
F-2401-2015REACTION RECOR: Amino Action- 500g (Island Breeze), Distributed by Reaction Nutrition, Carnegie, PA1,194Class IITerminated17 Jun 2015

Context

46%of 2015 food events are Class II607 events that year
13product records in this eventfirm median: 13
2events on this register for the firm

Other enforcement events for Reaction Nutrition LLC

InitiatedProduct (first record)TypeClassRecords
7 Nov 2012Clinical LIVE Dietary Supplement Immune Support 694.325 mg 90 capsules Distributed by Reaction Nutrition, LLC., Carnegie (65982)FoodClass I1

Questions and answers

Why was this food recalled?

FDA's record gives the reason for recall as: "Work out support nutritional supplements manufactured on shared equipment may contain unknown amounts of whey protein and soy."

What does Class II mean?

FDA classifies recalls by relative degree of health hazard. Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.

Where was the product distributed?

FDA's distribution pattern field reads: "nationwide to retailers and consumers"

Is the recall still ongoing?

FDA lists the status as Terminated; the termination date is 21 Nov 2018. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.

Where does this data come from?

openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.

Provenance

Source: openFDA food enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.