Crabmeat Lump Blend (Chicken of the Sea) – temperature abuse (2017)
Class II: 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
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Chicken of the Sea Pasteurized Crabmeat Lump Blend, Item #411820; Chicken of the Sea Pasteurized Crabmeat Claw, Item #370810; Jack's Catch Pasteurized Crabmeat Jumbo Lump Item #193980; Jack's Catch Pasteurized Crabmeat Lump, Item #199830. All packaged in 1 LB or 16 OZ tin cans.
Brand
Performance Food Group, Inc.
Lot Codes / Batch Numbers
Item #193980 Manufacturer Code Number: 93981-10 and Best by Date: 10/08/2018, Item #411820 Manufacturer Code Number: 411821238 and Best by Date(s): 09/02/2018, 10/28/2018, 11/08/2018, Item #370810 Manufacturer Code Number: 10843237008152 and Best by Date(s): 09/19/2018, 11/18/2018, Item #199830 Manufacturer Code Number: 93982-10 and Best by Date: 10/03/2018
Products Sold
Item #193980 Manufacturer Code Number: 93981-10 and Best by Date: 10/08/2018; Item #411820 Manufacturer Code Number: 411821238 and Best by Date(s): 09/02/2018; 10/28/2018; 11/08/2018; Item #370810 Manufacturer Code Number: 10843237008152 and Best by Date(s): 09/19/2018; 11/18/2018; Item #199830 Manufacturer Code Number: 93982-10 and Best by Date: 10/03/2018
Performance Food Group, Inc. is recalling Chicken of the Sea Pasteurized Crabmeat Lump Blend, Item #411820; Chicken of the Sea Pasteurized Cra due to The firm is initiating a recall due to potential temperature abuse to product during transit.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The firm is initiating a recall due to potential temperature abuse to product during transit.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CO, LA, MO, NE, OK, TX
Page updated: Jan 6, 2026