Murry's Hash Brown Potato Patties, packaged in cardboard trays covered with plastic…
Lamb Weston Inc recalled this product and the FDA reported the enforcement action on 10 October 2018 as Class II. The recall was initiated by the firm. Hash brown product, sold under brand Murry's is recalled because the product may contain small fragments of hard, clear plastic.
The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- Product
- Murry's Hash Brown Potato Patties, packaged in cardboard trays covered with plastic film, frozen products. -Tray UPC 0 73744 04001 4, retail packaged in 40.5 OZ (2.53 LB) (1.14 kg). -Case item M06, case UPC 1 00 73744 04001 1, case net wt. 30.375 LBS. (13.8 kg) ***Packed for: MURRY's INC. 7852 Walker Dr., Suite 420 Greenbelt, MD 20770***".
- UPC
- 073744040014
- Reason for recall
- Hash brown product, sold under brand Murry's is recalled because the product may contain small fragments of hard, clear plastic.
- Recalling firm
- Lamb Weston Inc
- Firm location
- Richland, Washington, United States
- Classification
- Class II
- Status
- Terminated
- Recall number
- F-0002-2019
- Quantity
- 2638 cases
- Distribution
- CA, FL, IA, MA, MD, OH, PA, and TX.
- Initiated
- 20 September 2018
- Reported by FDA
- 10 October 2018
- Terminated
- 14 December 2018
- Firm notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Product codes
- ***Murry's Hash Brown Potato Patties: Tray code: 60508061HH SELL BY SEP022019 Tray code: 60508062HH SELL BY SEP032019 Tray code: 60508073HH SELL BY SEP142019 Tray code: 60508074HH SELL BY SEP152019 Case Code: 6050806121HH:MM SELL BY SEP022019 Case Code: 6050806221HH:MM SELL BY SEP032019 Case Code: 6050807332HH:MM SELL BY SEP142019 Case Code: 6050807432HH:MM SELL BY SEP152019
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class II means the FDA judged a remote probability of serious harm, or a probability of temporary or medically reversible harm. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This is one of 2 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 2 separate recalls, which almost every published figure does, overstates it by a factor of 2. Every product code in this event is listed together on the record that covers the whole recall, which is the page a search engine is pointed to for all 2 of them.
- The recall ran for 3 months, from 20 September 2018 to termination on 14 December 2018. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
- The distribution pattern names 8 states, and the FDA published the enforcement report 3 weeks after the firm began the recall.
- The product description on this record names no food this site can classify, so it appears on no food-type page. That is a limit of the description rather than of the recall.
Named in the distribution pattern: California, Florida, Iowa, Massachusetts, Maryland, Ohio, Pennsylvania, Texas. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
What this recall was for
Foreign material
A foreign material recall means something that is not food was found in food: metal, plastic, glass, wood or insect matter, usually shed by equipment during processing.
A preventive controls plan covers foreign material under the clauses below. This is where the control belongs, not a finding against any firm named on this page: a recall record states a reason, and most of these recalls were initiated by the firm itself.
- 21 CFR 117.40
- Equipment and utensils: plant equipment designed and maintained so it cannot contaminate food with lubricants, fuel, metal fragments or contaminated water.
- 21 CFR 117.80(c)
- Manufacturing operations: the measures that protect food from contamination during processing, including the effective ones against metal and other extraneous material.
- 21 CFR 117.150
- Corrective actions: what a facility does when a preventive control was not properly implemented, including identifying and correcting the problem and evaluating the food for safety.
Other records from Lamb Weston Inc
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 9 other records name this firm.
All 10 records for Lamb Weston Inc
All 2018 recalls · All FDA food recall data
21 CFR 117.40 is the clause behind this recall, and it is one somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.