If the company making it says so,
according to the FDA
Recycled content in food packaging is increasing as sustainability advocates press manufacturers to cut their use of virgin plastic.
Since 1990, the U.S. Food and Drug Administration (FDA), the agency responsible for ensuring food contact materials are safe, approved at least 347 voluntary manufacturer applications for food contact materials made with recycled plastic, according to a database on its website. Approvals have tripled in recent years, from an average of 7 to 8 per year through 2019, to 23 per year since then, and they continue to climb. The FDA has already approved 27 proposals through June this year.
Other
than Coca-Cola, most manufacturers seeking approval are petrochemical giants
such as Eastman Chemicals, Dupont and Indorama; and lesser-known plastic
packaging manufacturers, including many from China, India and other countries.
The
end buyers of the recycled materials aren’t included in the FDA database, but
many popular brands are using recycled content. Cadbury chocolate bars come in
a wrapper marketed as 30% percent recycled “soft plastic packaging.” The
Coca-Cola Co. in North America reports it sells soft drinks in 100% percent recycled PET (polyethylene terephthalate)
bottles, while General Mills says its Annie’s cereal boxes use a liner made
from 35% percent recycled plastic film.
Increasing recycled content in packaging may be good news for the planet, but researchers say the FDA has a lax approval process for plastic food packaging that hasn’t kept pace with the science on chemical hazards in plastics. The agency's approval process for recycled plastics is voluntary and ignores the potential risk of chemical mixtures, researchers told EHN. Companies can seek guidance on their recycling process, but they are not required to.
In addition,
the FDA relies on manufacturers’ test data when it approves materials, leaving
companies essentially in charge of policing themselves. Meanwhile, some studies
show that recycled plastic can harbor even more toxic chemicals — such as bisphenol-A (BPA), phthalates,
benzene and others — than virgin plastic.
FDA
spokesperson Enrico Dinges defended the process, telling EHN the
agency “reviews [industry] data against stringent scientific guidelines” and
can “use its resources to spot test materials” if it sees an issue.
But
researchers say the agency fails to protect the public from the toxic chemical
soup found in recycled plastics.
“[The]
FDA is most concerned about pathogen contamination coming with the recycled
material, rather than chemicals,” Maricel Maffini told EHN. The
approval process “is very lax,” she said.
Recycled plastic is more toxic
Globally,
just 9% of plastic is recycled. Most is recycled mechanically, by sorting,
washing, grinding and re-compounding the material into pellets.
Most
recycling centers collect a mix of materials, allowing milk jugs, say, to
intermingle with detergent bottles or pesticide containers and potentially
absorb the hazardous chemicals from those non-food containers. Recycling
facilities that are set up to collect one plastic type, such as PET bottles,
can better control potential contamination, although chemicals could still be
introduced from bottle caps or the adhesives in labels.
Hazardous
chemicals can also be introduced when plastics are decontaminated and stabilized during recycling. Plastics degrade with
recycling, “so you may need to add more stabilizers to make the material as
robust as the virgin material,” Birgit Geueke, senior scientific officer at the
non-profit Food Packaging Forum, told EHN. “Recycling can therefore
increase the material complexity and the presence of different additives and
degradation products.”
Geueke,
who led a review of more than 700 studies on chemicals in
plastic food contact items, said that research on recycled plastics is limited.
Despite that caveat, “there are a few studies really showing that contamination
can be introduced more easily if you use recycled content.”
One study found 524 volatile organic chemicals in recycled
PET versus 461 in virgin PET. Chemicals detected in the recycled PET included
styrene, benzene, BPA, antimony,
formaldehyde and phthalates — chemicals linked to an array of health issues,
including cancer, the ability to hack hormones and development delays in
children, obesity and reproductive problems.
“Recycling
can therefore increase the material complexity and the presence of different
additives and degradation products.” — Birgit Geueke, Food Packaging Forum
Most
studies have focused on recycled PET, which is “not as prone to picking
chemicals up,” in comparison to other plastics such as recycled high-density
polyethylene (HDPE) and polypropylene, or PP, Geueke said. “HDPE milk bottles
really take up chemicals during all stages of their life cycle, much more than
PET bottles, and [those chemicals] are harder to remove, because they stick
harder to the material,” she said.
Indeed,
a study on recycled HDPE pellets obtained from various
countries in the Global South identified pesticides, pharmaceuticals and
industrial chemicals in the pellets.
FDA’s lax approach
The
FDA must authorize all materials that contact food before they reach the
market. To be authorized, a material cannot contain intentionally added
cancer-causing chemicals nor any other chemicals that leach from the material
at a level of more than 0.5 parts per billion.
But
as Maffini pointed out, the FDA recommends, but does not
require, the type of testing that manufacturers should do to ensure their
products are safe, and it doesn’t always require them to submit any safety
data, she said.
“If
you tell the FDA the substance or substances used to make the plastic are not
mutagenic or genotoxicant, and the exposure in the diet would be less than 0.5
parts per billion, FDA does not expect you to send any safety data [to back up
these claims].”
In
defense, the agency’s Dinges said, “the FDA has robust guidelines for the
underlying scientific data that should be provided” by industry. But he also
said, “it is the responsibility of the manufacturer to ensure that their
material meets all applicable specifications.”
For
recycled plastics, companies may also voluntarily submit a requested review of
their recycling process. In this case, the FDA asks companies to provide a
description of the process, test results showing that the process removes
possible incidental contamination and a description of how the material will be
used.
The
FDA further advises manufacturers to conduct “surrogate testing,” which
involves challenging recycled materials with, or submerging them into,
different classes of hazardous chemicals that could theoretically contaminate
the plastic, to determine whether the company’s recycling processes can
eliminate those toxic chemicals.
Surrogate
testing is the “best available practice” for evaluating chemical migration from
recycled plastics, Gueke said, although research shows it works better for PET
than for other plastics like PP or HDPE. But the FDA doesn’t require it.
According
to the FDA database of recycled plastic applications, two-thirds of the
approvals are for recycled PET, for a broad range of products from drink
bottles to clam shell containers for fruits and vegetables to tea bags. Most of
the remaining approvals are for recycled PP for products including clam shells,
disposable tableware, cutlery, caps and lids; recycled HDPE for grocery bags,
milk and juice bottles, meat trays and disposable tableware and recycled
polystyrene (PS) for meat and poultry trays and clam shells.
Most
requests are for mechanical recycling processes, though a couple dozen were
submitted for chemical recycling, which uses an energy intensive, largely unproven, process to convert plastics back to their
original monomer chemicals. [The FDA no longer evaluates chemical recycling
proposals for PET because it says the process produces material of suitable purity
for food-contact use.]
Outdated
approach to evaluating toxics
“The
FDA has been very reluctant to adopt a modern perspective,” Tom Zoeller,
professor emeritus at the University of Massachusetts Amherst, told EHN,
referring to testing for the effects of endocrine disruptors or for the
mixtures of chemicals found in plastics.
FDA’s
requirement that a chemical not exceed a threshold of 0.5 ppb is based on
cancer risk, Zoeller said, and while that number is protective for evaluating
exposure to a single chemical, “I'm not sure that means a lot, when you
consider the 16,000 chemicals that are put in plastic.”
In
other words, the FDA’s approach doesn’t account for multiple chemical
exposures, even as research shows that chemical mixtures can have significant
health impact. A European study, for instance, found that a mixture of nine different
chemicals had a greater impact on children's IQ than what was expected based on
individual risk assessments.
“It’s
the combination of chemicals that are impacting IQ and basically stealing human
potential,” Zoeller said. “We are way behind the curve,” in assessing chemical
risks, he added.
Dinges
responded that “while it is unlikely that appropriately sourced and controlled
feedstock will experience incidental contamination to any appreciable amount,
potential incidental contamination is addressed by the FDA’s surrogate testing
recommendations.”
Yet
the ability to control feedstock is what worries experts. Researchers who found BPA and heavy metals migrating at higher levels
from recycled PET compared to virgin PET, stressed that the plastic’s safety
depends on transparency and cooperation across the value chain. Moreover,
surrogate testing is not required.
“The
FDA has been very reluctant to adopt a modern perspective.” — Tom Zoeller,
University of Massachusetts Amherst
Neither
does FDA’s approach account for endocrine-disrupting chemicals, which can act
at levels in the parts per trillion by disrupting metabolism, Maffini and
Zoeller commented. “This concept that there's a threshold below which there are
no effects or no adverse effects is fundamentally incorrect,” said Zoeller.
Dinges
countered that the “effects on the endocrine system are just one of many areas
of toxicology that the FDA evaluates,” while also repeating industry talking
points. “Endocrine activation … does not necessarily translate into toxicity,”
he wrote. “Consumption of any food (for example, sugar) can activate the
endocrine system.”
Such
responses have led Zoeller to conclude that FDA has “become a foil for
industry,” and that their “precautionary principle is applied to industry, not
public health.”
Unless
government agencies can do a better job at ensuring manufacturers are keeping
chemical hazards out of recycled plastic, experts think it shouldn’t be used
for food contact materials.
“I'm
not a big fan of recycled plastic and food contact, because it's really hard to
know [if it’s safe], and I think producers have to be more careful than when
they produce virgin materials,” Geueke said, adding that she thinks that only
recycled PET should be considered because the other types so readily absorb
chemical contaminants.
“If
you have a very good process and can prove that it gets rid of most of the
contaminants…but nobody knows whether that really happens or not,” she said.
Meg Wilcox is an environmental journalist and photographer, covering climate change and energy, environmental health, fisheries management and sustainable food systems.